Medical Device Manufacturer · US , Simi Valley , CA

Hammer-Plane, Inc.

2 submissions · 2 cleared · Since 1993
2
Total
2
Cleared
0
Denied

Hammer-Plane, Inc. — FDA 510(k) Submissions

Hammer-Plane, Inc. has submitted 2 FDA 510(k) premarket notifications since 1993, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Fixation, Tracheal Tube, Arterial Blood Sampling Kit . Use the specialty filter in the sidebar to narrow results.

2 devices
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