Clearance Summary
XP202 received FDA 510(k) clearance under submission number K161922, sponsored by 3M Deutschland GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-09-01.
- Submission: K161922
- Applicant / Sponsor: 3M Deutschland GmbH
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2016-09-01
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.