Medical Device Manufacturer · US , New York , NY

Broadwest Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1985

Total

Cleared

Denied

Broadwest Corp. has 6 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 6 cleared submissions from 1985 to 1987. Primary specialty: General Hospital.

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

Broadwest Corp. 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 - Broadwest Corp.

6 devices

1-6 of 6