Neurosim Limited is one of 80 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Neurosim Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Neurosim Limited has 1 FDA 510(k) cleared medical devices. Based in Victoria, AU.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Neurosim Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neurosim Limited
1 devices