Clearance Summary
ELECTROmatic received FDA 510(k) clearance under submission number K163317, sponsored by Kaltenbach & Voigt Gmgh. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-02-21.
- Submission: K163317
- Applicant / Sponsor: Kaltenbach & Voigt Gmgh
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2017-02-21
Classification & Regulation
This clearance is catalogued under FDA product code EBW and 21 CFR 872.4200, within the Dental review panel as a Class I device.