Medical Device Manufacturer · DE , Hamburg

Weinmann Emergency Medical Technology GmbH + Co. KG

1 submissions · 1 cleared · Since 2020
1
Total
1
Cleared
0
Denied

Weinmann Emergency Medical Technology GmbH + Co. KG — FDA 510(k) Submissions

Weinmann Emergency Medical Technology GmbH + Co. KG has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Emergency, Powered (resuscitator) . Use the specialty filter in the sidebar to narrow results.

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