Clearance Summary
LAZERSMILE, LAZERWHITE received FDA 510(k) clearance under submission number K000290, sponsored by Biolase Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-04-14.
- Submission: K000290
- Applicant / Sponsor: Biolase Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6855
- Decision date: 2000-04-14
Classification & Regulation
This clearance is catalogued under FDA product code EFW and 21 CFR 872.6855, within the Dental review panel as a Class I device.