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Endo 6:1, T1 Line Endo 6 L, SIRONiTi Apex, T1 Spray

K150750 Class I Traditional
Decision Date
2015-07-02
Sponsor / Applicant
Sirona Dental Systems GmbH

Technical Specification

510(k) Submission ID K150750
Product Code EGS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2015-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Endo 6:1, T1 Line Endo 6 L, SIRONiTi Apex, T1 Spray received FDA 510(k) clearance under submission number K150750, sponsored by Sirona Dental Systems GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-07-02.

Classification & Regulation

This clearance is catalogued under FDA product code EGS and 21 CFR 872.4200, within the Dental review panel as a Class I device.