Clearance Summary
CRYSTALEYE SPECTROPHOTOMETER/CRYSTALEYE BASIC SET, MODEL CE100-DC/US received FDA 510(k) clearance under submission number K072643, sponsored by Olympus Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2007-11-16.
- Submission: K072643
- Applicant / Sponsor: Olympus Corporation
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3661
- Decision date: 2007-11-16
Classification & Regulation
This clearance is catalogued under FDA product code KZN and 21 CFR 872.3661, within the Dental review panel as a Class II device.