Clearance Summary
PIEZON MASTER 400 received FDA 510(k) clearance under submission number K896749, sponsored by Electro Medical Systems (Ems Sa). The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1990-08-31.
- Submission: K896749
- Applicant / Sponsor: Electro Medical Systems (Ems Sa)
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4850
- Decision date: 1990-08-31
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.