Clearance Summary
SINUSCOPE received FDA 510(k) clearance under submission number K940317, sponsored by Stephen Chakoff, 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 1995-05-24.
- Submission: K940317
- Applicant / Sponsor: Stephen Chakoff, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4760
- Decision date: 1995-05-24
Classification & Regulation
This clearance is catalogued under FDA product code EOB and 21 CFR 874.4760, within the Ear, Nose, Throat review panel as a Class II device.