Clearance Summary
DIAMOND LUSTRE received FDA 510(k) clearance under submission number K840254, sponsored by Jelrus Technical Products Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1984-04-25.
- Submission: K840254
- Applicant / Sponsor: Jelrus Technical Products Corp.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6030
- Decision date: 1984-04-25
Classification & Regulation
This clearance is catalogued under FDA product code EJR and 21 CFR 872.6030, within the Dental review panel as a Class I device.