Thermopeutix, Inc. is one of 5171 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thermopeutix, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Thermopeutix, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 5 cleared submissions from 2008 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Thermopeutix, Inc. Filter by specialty or product code using the sidebar.
Thermopeutix, Inc. — FDA 510(k) Products and Clearance History
5 devices
Cleared
Sep 26, 2013
PRIMI SUPPORT CATHETER
Cardiovascular
28d
Cleared
Jun 25, 2013
PRIMI AND SECONDI SUPPORT CATHETERS
Cardiovascular
90d
Cleared
Nov 18, 2011
TAPAS CATHETER
Cardiovascular
108d
Cleared
Aug 25, 2010
DUFLO CATHETER (HEPARIN COATED)
Cardiovascular
252d
Cleared
Sep 26, 2008
DUOFLO CATHETER
Cardiovascular
199d