Clearance Summary
F.G. LASER (DENTAL BUR) received FDA 510(k) clearance under submission number K901262, sponsored by Diamond Rotary and Carbide Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1990-07-09.
- Submission: K901262
- Applicant / Sponsor: Diamond Rotary and Carbide Intl.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4535
- Decision date: 1990-07-09
Classification & Regulation
This clearance is catalogued under FDA product code DZP and 21 CFR 872.4535, within the Dental review panel as a Class I device.