Clearance Summary
MAICO MA53 received FDA 510(k) clearance under submission number K981142, sponsored by Bernafon-Maico, Inc.. 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 1998-04-22.
- Submission: K981142
- Applicant / Sponsor: Bernafon-Maico, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1050
- Decision date: 1998-04-22
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.