Medical Device Manufacturer · US , Northridge , CA

Endoscopix - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990

Total

Cleared

Denied

Endoscopix has 1 FDA 510(k) cleared medical devices. Based in Northridge, US.

Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Gastroenterology & Urology.

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

1 devices

1–1 of 1