Clearance Summary
MODIFICATION TO: CERCON BASE received FDA 510(k) clearance under submission number K051462, sponsored by Dentsply Intl.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-06-24.
- Submission: K051462
- Applicant / Sponsor: Dentsply Intl.
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2005-06-24
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.