AC3 Series Intra-Aortic Balloon Pump (IABP)
Nov 2019
85d
Arrow International, Teleflex
1
Total
1
Cleared
0
Denied
Arrow International, Teleflex — FDA 510(k) Submissions
Arrow International, Teleflex has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Balloon, Intra-aortic And Control . Use the specialty filter in the sidebar to narrow results.
1 devices