Medical Device Manufacturer · CA , Westmount, Quebec

Stellate Systems - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1991

Total

Cleared

Denied

Stellate Systems has 7 FDA 510(k) cleared medical devices. Based in Westmount, Quebec, CA.

Historical record: 7 cleared submissions from 1991 to 2011. Primary specialty: Neurology.

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

Stellate Systems is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Stellate Systems

7 devices

1-7 of 7