Medical Device Manufacturer · US , Andover , MA

Endoscopy Division - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Endoscopy Division General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Jan 23, 1998

SMITH & NEPHEW DYONICS ARTHOSCOPES/ENDOSCOPES, SMITH & NEPHEW DYONICS...

General & Plastic Surgery · 32d