Medical Device Manufacturer · DE , Berlin

Rosch AG Medizintechnic - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Total

Cleared

Denied

Rosch AG Medizintechnic has 1 FDA 510(k) cleared medical devices. Based in Berlin, DE.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Rosch AG Medizintechnic Filter by specialty or product code using the sidebar.

Rosch AG Medizintechnic is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Rosch AG Medizintechnic

1 devices

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