Medical Device Manufacturer · US , North Attleboro , MA

Schott North America - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2011

Recent clearances: LIGHT GUIDE CABLE

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Schott North America General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Nov 25, 2011

LIGHT GUIDE CABLE

General & Plastic Surgery · 196d