Medical Device Manufacturer · US , Chelmsford , MA

Arrow International, Teleflex - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2019

1

Total

1

Cleared

0

Denied

FDA 510(k) cleared devices by Arrow International, Teleflex Cardiovascular ✕

1 devices

1-1 of 1

Cleared Nov 12, 2019

AC3 Series Intra-Aortic Balloon Pump (IABP)

Cardiovascular · 85d