Arrow International, Teleflex is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow International, Teleflex - FDA 510(k) Cleared Devices
Recent clearances: AC3 Series Intra-Aortic Balloon Pump (IABP)
1
Total
1
Cleared
0
Denied
Arrow International, Teleflex has 1 FDA 510(k) cleared medical devices. Based in Chelmsford, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arrow International, Teleflex Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arrow International, Teleflex
1 devices