Medical Device Manufacturer · US , Research Triangle Pa , NC

Weck Endoscopy - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1993

Total

Cleared

Denied

Weck Endoscopy has 4 FDA 510(k) cleared medical devices. Based in Research Triangle Pa, US.

Historical record: 4 cleared submissions from 1993 to 1993. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Weck Endoscopy Filter by specialty or product code using the sidebar.

Weck Endoscopy is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Weck Endoscopy

4 devices

1-4 of 4