Medical Device Manufacturer · DE , Dusseldorf

Miacom Diagnostics GmbH

1 submissions · 1 cleared · Since 2015
1
Total
1
Cleared
0
Denied

Miacom Diagnostics GmbH — FDA 510(k) Submissions

Miacom Diagnostics GmbH has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Kit, Identification, Enterobacteriaceae . Use the specialty filter in the sidebar to narrow results.

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All1 Microbiology 1