Medical Device Manufacturer · US , St. Louis , MO

Smith & Nephew Equipment Group - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1991

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Smith & Nephew Equipment Group General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Apr 02, 1991

SHAMPAINE MODEL 3800 OR MURANAKA MODEL OR-604M

General & Plastic Surgery · 36d

Cleared Jan 16, 1991

SHAMPAINE 1000 SERIES ANGENIEUX AX-14 DUO,AX-4

General & Plastic Surgery · 72d