Thermor , Ltd. is one of 204 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Thermor , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Thermor , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Newmarket, CA.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Thermor , Ltd. Filter by specialty or product code using the sidebar.
Thermor , Ltd. — FDA 510(k) Products and Clearance History
1 devices