Clearance Summary
CRYSTALLINE L3 MULTI-USE HYBRID COMPOSITE received FDA 510(k) clearance under submission number K935714, sponsored by Confi-Dental Products Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-01-21.
- Submission: K935714
- Applicant / Sponsor: Confi-Dental Products Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3750
- Decision date: 1994-01-21
Classification & Regulation
This clearance is catalogued under FDA product code DYH and 21 CFR 872.3750, within the Dental review panel as a Class II device.