Medical Device Manufacturer · DE , Koln

Servox Medizintechnik GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Recent clearances: MEDIPORT 2000 MOBILE

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Servox Medizintechnik GmbH General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jan 28, 2002

MEDIPORT 2000 MOBILE

General & Plastic Surgery · 90d