Medical Device Manufacturer · US , Monroe , MI

Nhr, Inc.

1 submissions · 1 cleared · Since 1994

Total

Cleared

Denied

Nhr, Inc. — FDA 510(k) Submissions

Nhr, Inc. has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

SKIN BIOPSY DEVICE

K933324 · MJG Device, Percutaneous, Biopsy · General & Plastic Surgery

Mar 1994 262d

Nhr, Inc.

Nhr, Inc. — FDA 510(k) Submissions

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