Eradlink, Inc. is one of 25260 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eradlink, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CR-PRO, LASERPRO 16
2
Total
2
Cleared
0
Denied
Eradlink, Inc. has 2 FDA 510(k) cleared medical devices. Based in Penn Valley, US.
Historical record: 2 cleared submissions from 2002 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Eradlink, Inc. 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 - Eradlink, Inc.
2 devices