meddevicedb.com FDA Device Reference

MBCP GEL

K060732 Class II Traditional
Decision Date
2006-06-02
Sponsor / Applicant
Biomatlante

Technical Specification

510(k) Submission ID K060732
Product Code LYC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3930
Decision Date 2006-06-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MBCP GEL received FDA 510(k) clearance under submission number K060732, sponsored by Biomatlante. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-06-02.

Classification & Regulation

This clearance is catalogued under FDA product code LYC and 21 CFR 872.3930, within the Dental review panel as a Class II device.