Pulsecor Limited is one of 5360 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulsecor Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pulsecor Limited has 1 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pulsecor Limited Filter by specialty or product code using the sidebar.
Pulsecor Limited — FDA 510(k) Products and Clearance History
1 devices