Dane Technologies is one of 21726 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dane Technologies - FDA 510(k) Cleared Devices
Recent clearances: DANE TECHNOLOGIES WHEELCHAIR MOVER, MODEL WM 2000
1
Total
1
Cleared
0
Denied
Dane Technologies has 1 FDA 510(k) cleared medical devices. Based in Brooklyn Park, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Dane Technologies 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 - Dane Technologies
1 devices