Medical Device Manufacturer · DE , Weisendorf

Rotec Medizintechnik GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Total

Cleared

Denied

Rotec Medizintechnik GmbH has 2 FDA 510(k) cleared medical devices. Based in Weisendorf, DE.

Historical record: 2 cleared submissions from 2000 to 2000. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Rotec Medizintechnik GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Rotec Medizintechnik GmbH

2 devices

1-2 of 2