Medical Device Manufacturer · US , New York , NY

Brilliant Ray Intl., Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1989

Total

Cleared

Denied

Brilliant Ray Intl., Inc. has 7 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 7 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

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

Brilliant Ray Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Brilliant Ray Intl., Inc.

7 devices

1-7 of 7