Arrow International, Inc. (Subsidiary of Telelflex Inc.) is one of 5582 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow International, Inc. (Subsidiary of Telelflex Inc.) - FDA 510(k)...
1
Total
1
Cleared
0
Denied
Arrow International, Inc. (Subsidiary of Telelflex Inc.) has 1 FDA 510(k) cleared medical devices. Based in Reading, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arrow International, Inc. (Subsidiary of Telelflex Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arrow International, Inc. (Subsidiary of Telelflex Inc.)
1 devices