Hotspur Technologies,Inc Subsidiary of Teleflex ME is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hotspur Technologies,Inc Subsidiary of Teleflex ME - FDA 510(k) Clear...
1
Total
1
Cleared
0
Denied
Hotspur Technologies,Inc Subsidiary of Teleflex ME has 1 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hotspur Technologies,Inc Subsidiary of Teleflex ME Filter by specialty or product code using the sidebar.
Hotspur Technologies,Inc Subsidiary of Teleflex ME — FDA 510(k) Products and Clearance History
1 devices