Clearance Summary
DENTATUS OSCIOMAT received FDA 510(k) clearance under submission number K031793, sponsored by Dentatus USA , 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 2003-11-13.
- Submission: K031793
- Applicant / Sponsor: Dentatus USA , Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4120
- Decision date: 2003-11-13
Classification & Regulation
This clearance is catalogued under FDA product code DZH and 21 CFR 872.4120, within the Dental review panel as a Class II device.