Medical Device Manufacturer · US , Springfield , VA

Reimers Systems, Inc.

5 submissions · 5 cleared · Since 1995
5
Total
5
Cleared
0
Denied

Reimers Systems, Inc. — FDA 510(k) Submissions

Reimers Systems, Inc. has submitted 5 FDA 510(k) premarket notifications since 1995, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Chamber, Hyperbaric . Use the specialty filter in the sidebar to narrow results.

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All5 Anesthesiology 5