Presented are systems and methods that provide diagnostic measurement tools that enable even laymen to reliably and accurately perform clinical-grade diagnostic measurements of key vital signs with little or no intervention by a health care professional. In various embodiments, this is accomplished by using an automated medical diagnostic system that provides clear and concise audio/video guidance to the patient and monitors the patient's equipment usage to generate high-accuracy measurement data that may be analyzed locally and shared with health care professionals and specialists, as needed.

A probe for ultrasound treatment of skin laxity are provided. Systems and methods can include ultrasound imaging of the region of interest for localization of the treatment area, delivering ultrasound energy at a depth and pattern to achieve the desired therapeutic effects, and/or monitoring the treatment area to assess the results and/or provide feedback. In an embodiment, a treatment system and method can be configured for producing arrays of sub-millimeter and larger zones of thermal ablation to treat the epidermal, superficial dermal, mid-dermal or deep dermal components of tissue.

An apparatus for acquiring signals from a pregnant subject includes a flexible portion that is conformable to an abdomen of the subject. The flexible portion includes a plurality of signal acquisition points, each signal acquisition point comprising a contact adapted to electrically couple to a respective electrode and signal acquisition circuitry. The flexible portion includes a first linear section that is generally aligned along a first axis; and a second linear section extending from the first linear section, the second linear section being generally aligned along a second axis that is perpendicular to the first axis; wherein a first group of the signal acquisition points is located along the first axis and a second group of the signal acquisition points is located along the second axis.

A method and system for noninvasive face lifts and deep tissue tightening are disclosed. An exemplary method and treatment system are configured for the imaging, monitoring, and thermal injury to treat the SMAS region. In accordance with an exemplary embodiment, the exemplary method and system are configured for treating the SMAS region by first, imaging of the region of interest for localization of the treatment area and surrounding structures, second, delivery of ultrasound energy at a depth, distribution, timing, and energy level to achieve the desired therapeutic effect, and third to monitor the treatment area before, during, and after therapy to plan and assess the results and/or provide feedback.

A method for guiding electrocardiogram (ECG) electrode placement on a person includes acquiring an image of the person, identifying an externally discernable anatomical landmark on the image, determining target locations for first through nth electrodes as a function of the location of the landmark, and highlighting the target locations on the person. A system for guiding placement of ECG electrodes comprises an imaging device, an illumination source, a processor, and machine readable instructions. The instructions, when executed by the processor, identify at least one marker in an image acquired by the imaging device, determine, as a function of the location of the at least one marker, target locations on the person at which first through nth ECG electrodes should be placed, and cause the illumination source to illuminate the first through nth target locations.

A method for operating an accessory device to capture calibration data. The method can include capturing an image of a portion of a user's body that includes the user's stoma and at least two reference locations, and storing distance scale information representative of a distance between the two reference locations. The method further includes processing the captured image, including: identifying the reference locations, identifying the stoma, and generating calibration data representative of one or more stoma parameters as a function of the identified reference locations, identified stoma and the distance scale information. The calibration data can be stored.

A clamp electrode apparatus comprises first and second clamps which are mechanically connected to form a single integrated device and arranged side by side such that a first edge of the first clamp faces a second edge of the second clamp. A channel is defined between the first and second edges for aligning a visible mark feature of a limb, such as a malleolus or ulnar head, within the opening or channel when the first and second clamps clamp the limb. When the limb is clamped with the clamp electrode apparatus multiple times, the visible mark feature can be aligned with reference to the channel. Thus, electrodes attached to the clamps contact generally the same locations even if the clamp electrode apparatus is removed after each measurement and is not kept on the limb throughout the multiple measurements.

A mobile electrocardiogram (ECG) device is described, comprising an electrode assembly comprising electrodes that sense heart-related signals when in contact with a body of a user, and produce electrical signals representing the sensed heart-related signals. The mobile ECG device further comprises a light-emitting device to facilitate an optimal placement of the electrode on the body of the user. The mobile ECG device further comprises a housing containing the electrode assembly, the converter assembly, the transmitter, and the light-emitting device. A first electrode of the electrode assembly forms a first side of the housing and comprises an opening through which the light-emitting device provides the UV light.

A system for measuring an angle of a joint of a user includes a center hub, a first arm, a second arm, a magnet, and a sensor. The center hub includes a first hub and a second hub. The first arm is configured for attachment to a first limb portion of the user at a first outer end and to the first hub at a first inner end. The second arm is configured for attachment to a second limb portion of the user at a second outer end and to the second hub at a second inner end, wherein the first hub is pivotally coupled to the second hub. The magnet is coupled to the second hub. The sensor is disposed in the center hub and configured to detect a rotation of the magnet.

There is provided an apparatus for positioning a front sensor and/or a back sensor across a thorax of a target individual, the apparatus comprising: a back positioning element comprising: a collar sized and shaped for fitting to a shoulder line and base of a back of a neck of the target individual, and an elongated element having a first end region connected to the collar, and a second end region with a location marker set to correspond to a target anatomical feature of the spine of the target individual, wherein when in use, the elongated element is positioned parallel to and over a long axis of a spine on the back of the target individual, and at least one front sensor and at least one back sensor are positioned on the thorax of the patient relative to the back positioning element for transmitting to and/or sensing from the target region.