Medical Device Manufacturer · US , Washington , DC

Pentapharm , Ltd.

2 submissions · 2 cleared · Since 2004
2
Total
2
Cleared
0
Denied

Pentapharm , Ltd. — FDA 510(k) Submissions

Pentapharm , Ltd. has submitted 2 FDA 510(k) premarket notifications since 2004, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plasma, Coagulation Control, Test, Time, Partial Thromboplastin . Use the specialty filter in the sidebar to narrow results.

2 devices
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