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MICROLUX/DL MICROLUX/BLU BIO/SCREEN

K121282 Class II Traditional
Decision Date
2012-07-24
Sponsor / Applicant
Addent, Inc.

Technical Specification

510(k) Submission ID K121282
Product Code NXV
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6350
Decision Date 2012-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROLUX/DL MICROLUX/BLU BIO/SCREEN received FDA 510(k) clearance under submission number K121282, sponsored by Addent, 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 2012-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code NXV and 21 CFR 872.6350, within the Dental review panel as a Class II device.