Medical Device Manufacturer · US , Walker , MI

Biermar AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1982

Total

Cleared

Denied

Biermar AG has 1 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 1 cleared submissions from 1982 to 1982. Primary specialty: Radiology.

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FDA 510(k) Regulatory Record - Biermar AG

1 devices

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