Clearance Summary
OptiComp received FDA 510(k) clearance under submission number K202920, sponsored by Pac-Dent, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2022-05-25.
- Submission: K202920
- Applicant / Sponsor: Pac-Dent, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3690
- Decision date: 2022-05-25
Classification & Regulation
This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.