Diamond Age Systems, Inc. is one of 25319 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diamond Age Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AZURYT MODEL CLT 1401, CO2 SURGICAL LASER SYSTEM
1
Total
1
Cleared
0
Denied
Diamond Age Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chandler, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Diamond Age Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Diamond Age Systems, Inc.
1 devices