Protec GmbH & Co. KG is one of 507 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Protec GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: OPTIMAX, COMPACT 2, OPTIMAX 2010, ECOMAX, OPTIMAX/ COMPACT 2
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Protec GmbH & Co. KG
2 devices