Medical Device Manufacturer · US , Palatine , IL

Cortek Endoscopy, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2000

Total

Cleared

Denied

Cortek Endoscopy, Inc. has 5 FDA 510(k) cleared medical devices. Based in Palatine, US.

Historical record: 5 cleared submissions from 2000 to 2000. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Cortek Endoscopy, Inc.

5 devices

1-5 of 5