Anrad Corp. is one of 25266 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anrad Corp. - FDA 510(k) Cleared Devices
Recent clearances: GR17 DIGITAL DETECTOR, DIGITAL DETECTOR, MODEL GR17
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.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Anrad Corp.
2 devices