A system for calibrating an analyzer includes a test strip body. The system further includes a plurality of leads on the test strip body. The system further includes a circuit on the test strip body. The circuit includes a first resistor interconnected with at least a first portion of the plurality of leads and a second resistor interconnected with at least a second portion of the plurality of leads. When the test strip body is inserted into an analyzer, the circuit is configured to provide a signal simulating an electrochemical test strip.

An electrochemical gas sensing element has a footprint of less than 5 mm×5 mm so the volume of electrolyte, the sizes of the electrodes, and the electrical interconnects are very small. This results in a fast stabilization after detecting gasses and enables rapid changes in bias voltage to target different gasses. The sensor body is ceramic, and the other components are stable at temperatures including solder reflow temperatures, thus allowing the use of conventional solder reflow techniques to mount the sensing element to a PCB. A sensor circuit is mounted on the sensing element body to detect the currents through the sensor electrode and digitally process the information, resulting in a more accurate analysis. The small size, low power consumption, and modularity allow the sensor element to be mounted in small handheld devices.

A detection system includes an electrochemical sensor. Measurement circuitry is coupled to the electrochemical sensor and configured to measure an electrical characteristic of the electrochemical sensor. A controller is coupled to the measurement circuitry and is configured to provide an indication based on the measured electrical characteristic. The controller is further configured to generate an electrical disturbance to the electrochemical sensor and obtain a sensor recovery profile to provide a diagnostic indication relative to the electrochemical sensor.

An inspection apparatus capable of performing responsivity inspection on a plurality of gas sensors at equivalent accuracies is provided. The inspection apparatus includes a plurality of inspected sensor disposing parts that are provided halfway through one gas flow path at equal intervals in an extending direction of the flow path and in each of which a gas sensor to be inspected is disposed, and a plurality of straightening plates provided upstream of each of the inspected sensor disposing parts on the gas flow path and separated at a constant distance from the inspected sensor disposing parts. The straightening plates each include a rectangular opening orthogonal to the gas flow path and open to the gas flow path. When the gas flow path extends in one direction in a horizontal plane, the opening has a longitudinal direction along a direction orthogonal to the one direction in the horizontal plane.

A sulfur oxide detection system includes an element part which includes a sensor cell and a diffusion regulating layer. The sensor cell includes a solid electrolyte layer, a first electrode arranged, and a second electrode. The sulfur oxide detection system also includes a voltage application circuit configured to apply a voltage to the sensor cell so that a potential of the second electrode becomes higher than a potential of the first electrode, and a current detection circuit configured to detect a current flowing between the first electrode and the second electrode. The sulfur oxide detection system further includes a controller coupled with the voltage application circuit and the current detection circuit, and configured to estimate a sulfur oxide concentration in a gas to which the first electrode is exposed by way of the diffusion layer.

Methods of determining a corrected analyte concentration in view of some error source are provided herein. The methods can be utilized for the determination of various analytes and/or various sources of error. In one example, the method can be configured to determine a corrected glucose concentration in view of an extreme level of hematocrit found within the sample. In other embodiments, methods are provided for identifying various system errors and/or defects. For example, such errors can include partial-fill or double-fill situations, high track resistance, and/or sample leakage. Systems are also provided for determining a corrected analyte concentration and/or detecting some system error.

A device and method for calibrating a NO delivery device using NO and NO.sub.2 measurements, without using a known standard.

To measure target component concentration in a liquid with higher accuracy without any dedicated apparatus or skill, a method is adapted to include: receiving a successive measurement value obtained by performing successive measurement of the target component concentration with use of a first measurement device immersed in the liquid; receiving a batch measurement value obtained by, with use of a second measurement device, performing batch measurement of the target component concentration in a part sampled from the liquid; and, when the batch measurement value is received, successively calculating a correlation value indicating the correlation between multiple successive measurement values and multiple batch measurement values respectively obtained in mutually corresponding multiple times of successive measurement and multiple times of batch measurement. In addition, the first measurement device is adapted to calculate the target component concentration or correct a successive measurement value with use of the latest correlation value.

A multi-gas detection apparatus is configured such that electric power supplied from a power supply to a heater is controlled by pulse width modulation so as to control the temperature of a first solid electrolyte body. The multi-gas detection apparatus detects the concentration of ammonia by using a first ammonia detection section in which an electromotive force is generated between a first reference electrode and a first detection electrode in accordance with the concentration of ammonia in the exhaust gas. The multi-gas detection apparatus calculates the amount of a change (i.e., offset voltage) in the ammonia electromotive force caused by change in the output voltage of the power supply. The multi-gas detection apparatus corrects the ammonia electromotive force generated in the first ammonia detection section through use of the calculated change amount.

An electrode cleaning and calibration system generally comprises a sensor holder assembly machined from a block of solid acrylic or similar plastic material, which can accommodate a variety of types and sizes of sensors for use in monitoring and measurement of water processing and treatment processes. Examples of sensors suitable for use in the system include pH sensors, dissolved oxygen sensors, chlorine sensors, ozone sensors, total suspended solid sensors, mixed liquor suspended solid sensors, ammonia sensors, monochloramine sensors, and ultraviolent transmittance sensors.