Clearance Summary
ADVANCED HAND HELD CO2 LASER/HH-550 FOR DGGD USE received FDA 510(k) clearance under submission number K864948, sponsored by Bio Quantum Technologies, 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 1987-03-30.
- Submission: K864948
- Applicant / Sponsor: Bio Quantum Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 1987-03-30
Classification & Regulation
This clearance is catalogued under FDA product code LNK and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.