Neurotherapies Reset GmbH is one of 440 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Neurotherapies Reset GmbH - FDA 510(k) Cleared Devices
Recent clearances: Desyncra for Tinnitus Therapy System, Desyncra for Tinnitus Pro System
1
Total
1
Cleared
0
Denied
Neurotherapies Reset GmbH has 1 FDA 510(k) cleared medical devices. Based in Juelich, DE.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Neurotherapies Reset GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Deborah L. Sheffield Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Neurotherapies Reset GmbH
1 devices