Neurosel (Medical) Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Neurosel (Medical) Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Neurosel (Medical) Limited has 1 FDA 510(k) cleared medical devices. Based in Andover, Hampshire, GB.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Neurosel (Medical) Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neurosel (Medical) Limited
1 devices