meddevicedb.com FDA Device Reference

QUEST 2 AND 20

K945910 Class II Traditional
Decision Date
1994-12-29
Sponsor / Applicant
Aalba Dent, Inc.

Technical Specification

510(k) Submission ID K945910
Product Code EJT
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3060
Decision Date 1994-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUEST 2 AND 20 received FDA 510(k) clearance under submission number K945910, sponsored by Aalba Dent, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code EJT and 21 CFR 872.3060, within the Dental review panel as a Class II device.