Arrow International, Inc. (Subsidiary of Teleflex is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow International, Inc. (Subsidiary of Teleflex - FDA 510(k) Cleare...
2
Total
2
Cleared
0
Denied
Arrow International, Inc. (Subsidiary of Teleflex has 2 FDA 510(k) cleared medical devices. Based in Reading, US.
Historical record: 2 cleared submissions from 2013 to 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Arrow International, Inc. (Subsidiary of Teleflex Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arrow International, Inc. (Subsidiary of Teleflex
2 devices