Clearance Summary
CAVITY VARNISH (INTERMEDIARY VARNISH AND DENTINAL TUBULI SEAL) received FDA 510(k) clearance under submission number K973919, sponsored by Medental Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1997-12-16.
- Submission: K973919
- Applicant / Sponsor: Medental Intl.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3260
- Decision date: 1997-12-16
Classification & Regulation
This clearance is catalogued under FDA product code LBH and 21 CFR 872.3260, within the Dental review panel as a Class II device.