Medical Device Manufacturer · US , New Orleans , LA

Bioceptive, Inc.

1 submissions · 1 cleared · Since 2014

Total

Cleared

Denied

Bioceptive, Inc. — FDA 510(k) Submissions

Bioceptive, Inc. has submitted 1 FDA 510(k) premarket notifications since 2014, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

Bioceptive Suction Cervical Retractor

K142204 · HDC Tenaculum, Uterine · Obstetrics & Gynecology

Dec 2014 130d

Bioceptive, Inc.

Bioceptive, Inc. — FDA 510(k) Submissions

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