Reliefband Technologies is one of 19020 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reliefband Technologies - FDA 510(k) Cleared Devices
Recent clearances: ReliefBand 1.5
1
Total
1
Cleared
0
Denied
Reliefband Technologies has 1 FDA 510(k) cleared medical devices. Based in Horsham, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Reliefband Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Whitman Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Reliefband Technologies
1 devices