Lenire Tinnitus Treatment Device— 510(k) DEN210033
UnknownNeuromod Devices Limited
FDA 510(k) clearance DEN210033 for Lenire Tinnitus Treatment Device, Unknown on 2023-03-06. Applicant: Neuromod Devices Limited. Device class: 2.
Clearance details
- Applicant
- Neuromod Devices Limited
- Product code
- Code QVN
- Device class
- Class 2
- Regulation
- 21 CFR 874.3410
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Dublin 8, IE
Data sourced from openFDA. This site is unofficial and independent of the FDA.