Medical Device Manufacturer · DE , Postfach 1266

Buttner-Frank GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1990

Total

Cleared

Denied

Buttner-Frank GmbH has 2 FDA 510(k) cleared medical devices. Based in Postfach 1266, DE.

Historical record: 2 cleared submissions from 1990 to 1990. Primary specialty: Obstetrics & Gynecology.

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FDA 510(k) Regulatory Record - Buttner-Frank GmbH

2 devices

1-2 of 2