Medical Device Manufacturer · US , Reading , PA

Arrow International (Subsidiary of Teleflex Inc.) - FDA 510(k) Cleare...

6 submissions · 6 cleared · Since 2012

Total

Cleared

Denied

Arrow International (Subsidiary of Teleflex Inc.) has 6 FDA 510(k) cleared medical devices. Based in Reading, US.

Historical record: 6 cleared submissions from 2012 to 2013. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Arrow International (Subsidiary of Teleflex Inc.) Filter by specialty or product code using the sidebar.

Arrow International (Subsidiary of Teleflex Inc.) is one of 5656 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.