Medical Device Manufacturer · DE , Fuerth, Bayern

Sohard AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Recent clearances: RADIN, MODEL V 3.0

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sohard AG Radiology ✕

1 devices

1-1 of 1

Cleared Jan 28, 2005

RADIN, MODEL V 3.0

Radiology · 42d