meddevicedb.com FDA Device Reference

Zone, ZoneFree, Zone A1

K151526 Class II Traditional
Decision Date
2015-09-10
Sponsor / Applicant
Sybron Dental Specialties

Technical Specification

510(k) Submission ID K151526
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 2015-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Zone, ZoneFree, Zone A1 received FDA 510(k) clearance under submission number K151526, sponsored by Sybron Dental Specialties. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-09-10.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.