Medical Device Manufacturer · US , Weatherford , OK

Ferrania USA, Inc.

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Ferrania USA, Inc. — FDA 510(k) Submissions

Ferrania USA, Inc. has submitted 1 FDA 510(k) premarket notifications since 2001, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

LIFERAY FW MAMMO CASSETTE, LIFERAY KW MAMMO CASETTE

K013229 · IXA Cassette, Radiographic Film · Radiology

Oct 2001 15d

Ferrania USA, Inc.

Ferrania USA, Inc. — FDA 510(k) Submissions

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