Sensortek, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Sensortek, Inc. makes
Sensortek, Inc. manufactures diagnostic and testing devices, including the NTE-2 Thermal Sensitivity Tester for evaluating thermal response, esophageal stethoscopes with electrical conductors for auscultation, thermocouple sensors for electronic temperature measurement, and the Vibratron II for vibration sensitivity testing.
The company’s portfolio includes Class I and Class II devices, with products authorised via the FDA’s 510(k) pathway. These devices are listed under the U.S. regulatory framework, and the manufacturer is based in the United States.
Catalogue
Nte-2 Thermal Sensitivity Tester Ref K864345
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Vibratron Ii, Vibration Sensitivity Tester Ref K863607
Regimes: 510(k) Registry: 510(k)Esophageal Stetho Scope Ref K844055
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sensortek, Inc. have in the registry?
The registry currently lists 5 devices for Sensortek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sensortek, Inc.'s devices?
Among its 5 most recently registered devices, Sensortek, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Sensortek, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Sensortek, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sensortek, Inc. in the registry?
The most recently registered devices listed for Sensortek, Inc. include NTE-2 THERMAL SENSITIVITY TESTER, ESOPHAGEAL STETHOSCOPE WITH ELECTRICAL CONDUCTORS, THERMOCOUPLE SENSORS, ACCESS. FOR ELECTRONIC THERM and VIBRATRON II, VIBRATION SENSITIVITY TESTER.