Medical Device Manufacturer · DE , Henningsdorf

Brahms GmbH

2 submissions · 1 cleared · Since 2016
2
Total
1
Cleared
1
Denied

Brahms GmbH — FDA 510(k) Submissions

Brahms GmbH has submitted 2 FDA 510(k) premarket notifications since 2016, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device To Detect And Measure Procalcitonin (pct) In Human Clinical Specimens, Procalcitonin Assay . Use the specialty filter in the sidebar to narrow results.

2 devices
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