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LRT ATTACHMENT

K112333 Class II Traditional
Decision Date
2012-01-30
Sponsor / Applicant
Bcf Certification, Inc.

Technical Specification

510(k) Submission ID K112333
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2012-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LRT ATTACHMENT received FDA 510(k) clearance under submission number K112333, sponsored by Bcf Certification, 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 2012-01-30.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.