Embodiments for local and safe testing of injection fluids by drawing a sample of injection fluid into a local test chamber while drawing fluid to be tested into a syringe assembly and testing the sample of the injection fluid are disclosed. A fluid test device can include a syringe assembly, a plunger assembly, and a test module. The test module can determine information about fluid in a syringe assembly when the fluid enters a test chamber in the test module. Fluid may enter the test chamber through a one-way valve while a plunger in the plunger assembly is moved in a suction stroke to draw fluid into an interior of the syringe assembly. Fluid may not enter or be expelled from the test chamber when the plunger does not move or is moved in a compression stroke to expel fluid from the syringe assembly.

The subject innovation relates to a device for determining the concentration of a base and here especially hydrogen carbonate, whereby the device contains at least one pH indicator, at least one solid acid, and a mixture of at least one anionic surfactant and one nonionic surfactant. In addition, the subject innovation relates to a method for measuring the base concentration using the device according the subject innovation and a method for increasing the sensitivity of a testing device.

Provided herein are systems and methods of assessing a concentration of iron in a body fluid sample, such as whole blood. Systems include a highly stable, fast reacting, and accurate sensing area of a sensor for contacting with a body fluid sample, wherein upon contact, the body fluid sample causes a color change to the sensor that correlates with the concentration of iron in the body fluid sample. The disclosed systems and methods generate one or more signal outputs of light intensity data, from which the concentration of iron in the body fluid sample is determined.

Color quantification of chemical test pads and titration of analytes can be performed under different lighting conditions. In one embodiment, the lighting condition is estimated under which a digital image is captured and utilized to select a set of reference colors from which the quantified color is compared to determine the titration. In another embodiment, a plurality of comparisons are made with different lighting conditions with the result having the highest confidence level being selected to determine the titration.

A system and method for evaluating the concentration of an analyte contained on a diagnostic device. The method includes preparing a database of a plurality of digital images of drug test strips showing different concentrations of analytes; preparing a machine learning model of the drug test strips; comparing an active diagnostic device to the machine learning model, and evaluating the concentration of analytes In the active diagnostic device by comparing the active diagnostic device drug panel to the drug panel of the machine learning model of a diagnostic device.

Provided is a test system operable with a simplified structure. A test system includes a first test device and a second test device each of which transports and tests a sample. The test device includes a master control unit, which performs assignment of samples to the first test device and the second test device, and control of a transport operation of the sample assigned to the test device. The test device includes a slave control unit, which controls a transport operation of the sample assigned to the test device by the master control unit.

A lateral flow assay device includes several markers, a color bar, and/or a grayscale on the housing of the lateral flow assay device. The markers are used to assist in focusing a mobile device's camera on the control line of the lateral flow assay device. The markers may be used to adjust the perspective of an image taken from the control line and the test line of the lateral flow assay device. The markers may be used to locate the images of the control line, the test line, the color bar, and/or the grayscale on the image. The image of the color bar and the grayscale may be used to adjust the colors and intensity of the image. The images of the test line and the control line may then be used to determine the test results of the lateral flow assay device.

An unmanned vehicle operated autonomously or by remotely piloting incorporates an onboard camera which is affixed with clear tape coated with a chemical colorimetric sensor dye sensitive to chemical warfare agents. Chemical warfare agents are detected by visual review or autonomous measurement of sensor color changes while the unmanned vehicle travels through a region suspected of having chemical warfare agents present. In various implementations, the sensor output color changes may be visually monitored by a vehicle operator viewing the camera image from a remote location. In various embodiments, the detection of chemical warfare agents may be confirmed by processing the coated tape with a calibrated opto-electronic reader.

A composition, which can prepare hypochlorous acid water having a pH of 5 to 7.5, a concentration of hypochlorous acid of 50 to 500 ppm, a concentration of free chlorine molecules lower than an effective chlorine concentration, the concentration of free chlorine molecules of 20 ppm or less, and a nonionized hypochlorous acid as an active ingredient when diluted with an aqueous vehicle, the composition comprising: 1) one or more selected from trichloroisocyanuric acid, dichloroisocyanuric acid and salts thereof; and 2) a buffer salt (provided that, a chlorite of an alkali metal or alkaline earth metal is included in neither the aqueous medium nor the composition).

Systems, methods, and apparatus are disclosed for determining quantitative hormone and chemical analyte results from qualitative test results. An image is taken of an ovulation test device. The image is analyzed to identify a color intensity ratio (T/C ratio) between a color density of a test-line to a color density of a control-line. Additionally, a quantitative substance level may be determined using the T/C ratio, by identifying the type of test device and referencing a data structure that relates quantitative substance levels to T/C ratios for the identified type of test device.