Clearance Summary
CAVIOS CAVITY LINER received FDA 510(k) clearance under submission number K111668, sponsored by Neodental Chemical Products Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2011-08-19.
- Submission: K111668
- Applicant / Sponsor: Neodental Chemical Products Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3250
- Decision date: 2011-08-19
Classification & Regulation
This clearance is catalogued under FDA product code EJK and 21 CFR 872.3250, within the Dental review panel as a Class II device.