Medical Device Manufacturer · US , Andover , MA

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

18 submissions · 17 cleared · Since 1996

18

Total

17

Cleared

0

Denied

FDA 510(k) Regulatory Record - Smith & Nephew Endoscopy, Inc. Gastroenterology & Urology ✕

2 devices

1-2 of 2

Cleared Jul 14, 1999

SMITH & NEPHEW SUTURE LOK

Gastroenterology & Urology · 76d

Cleared Aug 06, 1997

SMITH & NEPHEW SUTURE COLLET

Gastroenterology & Urology · 71d