Clearance Summary
Piezon Built-in Kit, Piezon Built-in Kit LED received FDA 510(k) clearance under submission number K191079, sponsored by E.M.S Electro Medical Systems S.A. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-08-16.
- Submission: K191079
- Applicant / Sponsor: E.M.S Electro Medical Systems S.A
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4850
- Decision date: 2019-08-16
Classification & Regulation
This clearance is catalogued under FDA product code ELC and 21 CFR 872.4850, within the Dental review panel as a Class II device.