Thermotek, Inc. is one of 20549 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thermotek, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VASCUCOMP, NANOTHERM, VASCUTHERM AND PROTHERMO THERAPY WRAPS, THERMOTEK H-300
4
Total
3
Cleared
0
Denied
Thermotek, Inc. has 3 FDA 510(k) cleared medical devices. Based in Carrollton, US.
Historical record: 3 cleared submissions from 1995 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Thermotek, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Thermotek, Inc.
4 devices