Medical Device Manufacturer · NL , 3981 Ae Bunnik

Mijnhardt B.V. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1995

Total

Cleared

Denied

Mijnhardt B.V. has 1 FDA 510(k) cleared medical devices. Based in 3981 Ae Bunnik, NL.

Historical record: 1 cleared submissions from 1995 to 1995. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Mijnhardt B.V. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Mijnhardt B.V.

1 devices

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