Clearance Summary
TRACOR MODEL RA 208 COMPLIANCE AUDIOM received FDA 510(k) clearance under submission number K760859, sponsored by Tracor Instruments, 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 1976-10-29.
- Submission: K760859
- Applicant / Sponsor: Tracor Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.1050
- Decision date: 1976-10-29
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.