Ampcare, LLC is one of 5158 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ampcare, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ampcare, LLC has 2 FDA 510(k) cleared medical devices. Based in Richardson, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Ampcare, LLC Filter by specialty or product code using the sidebar.
Ampcare, LLC — FDA 510(k) Products and Clearance History
2 devices
Cleared
Oct 31, 2013
AMPCARE ESP THERAPY SYSTEM
Physical Medicine
184d
Cleared
Oct 15, 2012
REUSABLE CUTANEOUS ELECTRODE
Neurology
150d