Medical Device Manufacturer · US , Andover , MA

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

8 submissions · 8 cleared · Since 2007
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Smith & Nephew Inc., Endoscopy Division General Hospital
1 devices
1-1 of 1
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