Medical Device Manufacturer · DE , Pfullendorf

Msi Medserv International Deutschland GmbH

1 submissions · 1 cleared · Since 2009
1
Total
1
Cleared
0
Denied

Msi Medserv International Deutschland GmbH — FDA 510(k) Submissions

Msi Medserv International Deutschland GmbH has submitted 1 FDA 510(k) premarket notifications since 2009, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices
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All1 Gastroenterology & Urology 1