Medical Device Manufacturer · US , Peabody , MA

Anrad Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Anrad Corp. has 2 FDA 510(k) cleared medical devices. Based in Peabody, US.

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

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

Anrad 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 - Anrad Corp.

2 devices

1-2 of 2