Medical Device Manufacturer · US , Portland , OR

Cogan Corp.

1 submissions · 1 cleared · Since 1992

Total

Cleared

Denied

Cogan Corp. — FDA 510(k) Submissions

Cogan Corp. has submitted 1 FDA 510(k) premarket notifications since 1992, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

COGAN CORP KITS OF DENTAL HAND INSTRUMENTS

K915299 · EGG Attachment, Precision, All · Dental

Jan 1992 73d

Cogan Corp.

Cogan Corp. — FDA 510(k) Submissions

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