Clearance Summary
'EXMOOR' DAS GUPTA LARYNGEAL KEEL received FDA 510(k) clearance under submission number K864936, sponsored by Exmoor Plastics , Ltd.. 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 1987-04-27.
- Submission: K864936
- Applicant / Sponsor: Exmoor Plastics , Ltd.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3620
- Decision date: 1987-04-27
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.