Medical Device Manufacturer · US , East Hills , NY

Pall Corp.

3 submissions · 3 cleared · Since 1998
3
Total
3
Cleared
0
Denied

Pall Corp. — FDA 510(k) Submissions

Pall Corp. has submitted 3 FDA 510(k) premarket notifications since 1998, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Apparatus, Autotransfusion, Filter, Blood, Cardiopulmonary Bypass, Arterial Line, Filter, Infusion Line . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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