Arrow International, Inc (Subsidiary of Teleflex I is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow International, Inc (Subsidiary of Teleflex I - FDA 510(k) Clear...
1
Total
1
Cleared
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Denied
Arrow International, Inc (Subsidiary of Teleflex I has 1 FDA 510(k) cleared medical devices. Based in Reading, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arrow International, Inc (Subsidiary of Teleflex I Filter by specialty or product code using the sidebar.
Arrow International, Inc (Subsidiary of Teleflex I — FDA 510(k) Products and Clearance History
1 devices