Medical Device Manufacturer · DE , Oberstenfeld

Protec GmbH & Co. KG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Protec GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Oberstenfeld, DE.

Historical record: 2 cleared submissions from 1999 to 2009. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Protec GmbH & Co. KG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Protec GmbH & Co. KG

2 devices

1-2 of 2