Medical Device Manufacturer · US , Chelmsford , MA

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

1 submissions · 1 cleared · Since 2019

Total

Cleared

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) cleared devices by Arrow International, Teleflex

1 devices

1-1 of 1