Sensortek, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Sensortek, Inc. has 5 FDA 510(k) cleared medical devices. Based in Clifton, US.
Historical record: 5 cleared submissions from 1984 to 1987. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Sensortek, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sensortek, Inc.
5 devices
Cleared
Jan 29, 1987
NTE-2 THERMAL SENSITIVITY TESTER
Neurology
86d
Cleared
Dec 03, 1986
VIBRATRON II, VIBRATION SENSITIVITY TESTER
Neurology
78d
Cleared
Sep 03, 1985
ESOPHAGEAL STETHOSCOPE WITH ELECTRICAL CONDUCTORS
Anesthesiology
104d
Cleared
Jan 09, 1985
THERMOCOUPLE SENSORS, ACCESS. FOR ELECTRONIC THERM
General Hospital
83d
Cleared
Oct 25, 1984
ESOPHAGEAL STETHO SCOPE
Anesthesiology
7d