Medical Device Manufacturer · US , Pleasanton , CA

Prospera Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2012
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.

FDA 510(k) Regulatory Record - Prospera Corporation

2 devices
1-2 of 2
Cleared Mar 28, 2013
PROSPERA OTC TENS ELECTRONIC PULSE MASSAGER
K122744 · NUH
Neurology · 202d
Cleared Jul 27, 2012
ELECTRONIC PULSE MASSAGER TENS ELECTRONIC PULSE MASSAGER
K113544 · GZJ
Neurology · 239d
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