Clearance Summary
ENDO-LASE CD-100 CO2 LASER FOR OTORHINOLARYNGOLOGY received FDA 510(k) clearance under submission number K853875, sponsored by Endo Lase, 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 1986-01-09.
- Submission: K853875
- Applicant / Sponsor: Endo Lase, Inc.
- Clearance pathway: Traditional
- Review panel: Ear, Nose, Throat
- Device class: Class II
- Regulation citation: 21 CFR 874.4500
- Decision date: 1986-01-09
Classification & Regulation
This clearance is catalogued under FDA product code EWG and 21 CFR 874.4500, within the Ear, Nose, Throat review panel as a Class II device.