Clearance Summary
AMERICAN DENTAL LASER SINGLE USE CONTACT 320 HANDP received FDA 510(k) clearance under submission number K923539, sponsored by American Dental Laser, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1992-10-28.
- Submission: K923539
- Applicant / Sponsor: American Dental Laser, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 1992-10-28
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.