Clearance Summary
HINT AUDIOMETER, OR HINT received FDA 510(k) clearance under submission number K003913, sponsored by Maico-Diagnostics. 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 2001-03-16.
- Submission: K003913
- Applicant / Sponsor: Maico-Diagnostics
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1050
- Decision date: 2001-03-16
Classification & Regulation
This clearance is catalogued under FDA product code EWO and 21 CFR 874.1050, within the Ear, Nose, Throat review panel as a Class II device.