Clearance Summary
KODAK 9000, KODAK 9000 3D received FDA 510(k) clearance under submission number K073435, sponsored by Trophy. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-02-11.
- Submission: K073435
- Applicant / Sponsor: Trophy
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.1800
- Decision date: 2008-02-11
Classification & Regulation
This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.