Fehling Instruments GmbH & Co. KG is one of 490 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Fehling Instruments GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: Biopsy Forceps, Fehling-Punches
2
Total
2
Cleared
0
Denied
Fehling Instruments GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Karlstein, DE.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fehling Instruments GmbH & Co. KG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Visamed GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Fehling Instruments GmbH & Co. KG
2 devices