Medical Device Manufacturer · US , Andover , MA

Smith & Nephew Dyonics, Inc. - FDA 510(k) Cleared Devices

22 submissions · 19 cleared · Since 1990

22

Total

19

Cleared

0

Denied

FDA 510(k) Regulatory Record - Smith & Nephew Dyonics, Inc. Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Aug 19, 1994

SMITH & NEPHEW DYONICS INC. ELECTRONIC ENDOSCOPE

Obstetrics & Gynecology · 242d