Clearance Summary
KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 received FDA 510(k) clearance under submission number K032081, sponsored by Kavo America. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-07-24.
- Submission: K032081
- Applicant / Sponsor: Kavo America
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2003-07-24
Classification & Regulation
This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.