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