Medical Device Manufacturer · DE , Karlstein

Fehling Instruments GmbH & Co. KG

2 submissions · 2 cleared · Since 2016
2
Total
2
Cleared
0
Denied

Fehling Instruments GmbH & Co. KG — FDA 510(k) Submissions

Fehling Instruments GmbH & Co. KG has submitted 2 FDA 510(k) premarket notifications since 2016, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Rongeur, Manual, Device, Biopsy, Endomyocardial . Use the specialty filter in the sidebar to narrow results.

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All2 Neurology 1 Cardiovascular 1