meddevicedb.com FDA Device Reference

Shaders ZR

K190569 Class II Traditional
Decision Date
2019-07-29
Sponsor / Applicant
Digital Age Dental Lab

Technical Specification

510(k) Submission ID K190569
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 2019-07-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Shaders ZR received FDA 510(k) clearance under submission number K190569, sponsored by Digital Age Dental Lab. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-07-29.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.