Endoscopy Division is one of 16306 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endoscopy Division - FDA 510(k) Cleared Devices
Recent clearances: SMITH & NEPHEW DYONICS ARTHOSCOPES/ENDOSCOPES, SMITH & NEPHEW DYONICS LAPAROSCOPES, SNITH & NEPHEW DYONICS HYSTEROSCOPES
1
Total
1
Cleared
0
Denied
Endoscopy Division has 1 FDA 510(k) cleared medical devices. Based in Andover, US.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Endoscopy Division Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Endoscopy Division
1 devices