Clearance Summary
DAWN LOW SPEED HANDPIECE SYSTEM received FDA 510(k) clearance under submission number K821484, sponsored by Young Dental Manufacturing Co. 1, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1982-06-09.
- Submission: K821484
- Applicant / Sponsor: Young Dental Manufacturing Co. 1, LLC
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 1982-06-09
Classification & Regulation
This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.