Clearance Summary
FONIX ,MODEL 8000 received FDA 510(k) clearance under submission number K093006, sponsored by Frye Electronics, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2009-12-30.
- Submission: K093006
- Applicant / Sponsor: Frye Electronics, Inc.
- Clearance pathway: Abbreviated
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.3310
- Decision date: 2009-12-30
Classification & Regulation
This clearance is catalogued under FDA product code ETW and 21 CFR 874.3310, within the Ear, Nose, Throat review panel as a Class II device.