Medical Device Manufacturer · US , Irvine , CA

Cervilenz, Inc.

1 submissions · 1 cleared · Since 2001

Total

Cleared

Denied

Cervilenz, Inc. — FDA 510(k) Submissions

Cervilenz, 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 Sound, Uterine . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

CERVILENZ UTERINE MEASURING SOUND

K011840 · HHM Sound, Uterine · Obstetrics & Gynecology

Aug 2001 59d

Cervilenz, Inc.

Cervilenz, Inc. — FDA 510(k) Submissions

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