Prospera Corporation is one of 5240 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prospera Corporation - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Prospera Corporation has 2 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Prospera Corporation Filter by specialty or product code using the sidebar.
Prospera Corporation — FDA 510(k) Products and Clearance History
2 devices
Cleared
Mar 28, 2013
PROSPERA OTC TENS ELECTRONIC PULSE MASSAGER
Neurology
202d
Cleared
Jul 27, 2012
ELECTRONIC PULSE MASSAGER TENS ELECTRONIC PULSE MASSAGER
Neurology
239d