Clearance Summary
Premier Sealant received FDA 510(k) clearance under submission number K161580, sponsored by Premier Dental Company Products. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-10-18.
- Submission: K161580
- Applicant / Sponsor: Premier Dental Company Products
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3765
- Decision date: 2016-10-18
Classification & Regulation
This clearance is catalogued under FDA product code EBC and 21 CFR 872.3765, within the Dental review panel as a Class II device.