Medical Device Manufacturer · FR , Rueil Malmaison Cedex

Novacor - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Novacor has 2 FDA 510(k) cleared medical devices. Based in Rueil Malmaison Cedex, FR.

Historical record: 2 cleared submissions from 2004 to 2005. Primary specialty: Cardiovascular.

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

Novacor is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Novacor

2 devices

1-2 of 2