Clearance Summary
MONTG. LARYNGEAL KEEL received FDA 510(k) clearance under submission number K842800, sponsored by Boston Medical Products, 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 1984-08-02.
- Submission: K842800
- Applicant / Sponsor: Boston Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3620
- Decision date: 1984-08-02
Classification & Regulation
This clearance is catalogued under FDA product code FWN and 21 CFR 874.3620, within the Ear, Nose, Throat review panel as a Class II device.