Medical Device Manufacturer · US , Crofton , MD

Perfusion Partners & Assoc., Inc.

2 submissions · 2 cleared · Since 2003
2
Total
2
Cleared
0
Denied

Perfusion Partners & Assoc., Inc. — FDA 510(k) Submissions

Perfusion Partners & Assoc., Inc. has submitted 2 FDA 510(k) premarket notifications since 2003, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Centrifuges (micro, Ultra, Refrigerated) For Clinical Use . Use the specialty filter in the sidebar to narrow results.

2 devices
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