Medical Device Manufacturer · US , Andover , MA

Endoscopy Division - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Recent clearances: SMITH & NEPHEW DYONICS ARTHOSCOPES/ENDOSCOPES, SMITH & NEPHEW DYONICS LAPAROSCOPES, SNITH & NEPHEW DYONICS HYSTEROSCOPES

1
Total
1
Cleared
0
Denied

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

1 devices
1-1 of 1
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