Ipulse Limited is one of 174 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Ipulse Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ipulse Limited has 1 FDA 510(k) cleared medical devices. Based in Swansea, GB.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ipulse Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ipulse Limited
1 devices