Medical Device Manufacturer · US , Peabody , MA

Anrad Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004
2
Total
2
Cleared
0
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.

FDA 510(k) Regulatory Record - Anrad Corp.
2 devices
1-2 of 2
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