Clearance Summary
RDT3 HANDPIECE HEAD MODEL RDT3 received FDA 510(k) clearance under submission number K101172, sponsored by Redent Nova, 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 2010-07-27.
- Submission: K101172
- Applicant / Sponsor: Redent Nova, Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2010-07-27
Classification & Regulation
This clearance is catalogued under FDA product code EFA and 21 CFR 872.4200, within the Dental review panel as a Class I device.