Medical Device Manufacturer · US , Warren , NJ

Cordis Corp., A Johnson & Johnson Co. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2006

Total

Cleared

Denied

Cordis Corp., A Johnson & Johnson Co. has 5 FDA 510(k) cleared medical devices. Based in Warren, US.

Historical record: 5 cleared submissions from 2006 to 2014. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cordis Corp., A Johnson & Johnson Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cordis Corp., A Johnson & Johnson Co.

5 devices

1-5 of 5