Clearance Summary
DR. DEDO'S FAMILY EAR EXAMINATION KIT received FDA 510(k) clearance under submission number K904659, sponsored by Panex Corp.. 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 1991-04-30.
- Submission: K904659
- Applicant / Sponsor: Panex Corp.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class I
- Regulation citation: 21 CFR 874.4770
- Decision date: 1991-04-30
Classification & Regulation
This clearance is catalogued under FDA product code ERA and 21 CFR 874.4770, within the Ear, Nose, Throat review panel as a Class I device.