Medical Device Manufacturer · US , Warren , NJ

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

4 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Cordis, A Johnson & Johnson Co. has 2 FDA 510(k) cleared medical devices. Based in Warren, US.

Historical record: 2 cleared submissions from 1999 to 2014. Primary specialty: Cardiovascular.

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

Cordis, A Johnson & Johnson Co. is one of 5132 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Cordis, A Johnson & Johnson Co. — FDA 510(k) Products and Clearance History

4 devices

1-4 of 4