Clearance Summary
TINNITUS SOUND GENERATOR MODULE received FDA 510(k) clearance under submission number K073636, sponsored by Gn Resound A/S. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2008-03-13.
- Submission: K073636
- Applicant / Sponsor: Gn Resound A/S
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3400
- Decision date: 2008-03-13
Classification & Regulation
This clearance is catalogued under FDA product code KLW and 21 CFR 874.3400, within the Ear, Nose, Throat review panel as a Class II device.