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MIRACLE MIX CAPS GLASS IONOMER CEMENT INCAPSULES

K913175 Class II Traditional
Decision Date
1991-12-27
Sponsor / Applicant
G-C Intl. Corp.

Technical Specification

510(k) Submission ID K913175
Product Code EJJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3070
Decision Date 1991-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MIRACLE MIX CAPS GLASS IONOMER CEMENT INCAPSULES received FDA 510(k) clearance under submission number K913175, sponsored by G-C Intl. Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1991-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code EJJ and 21 CFR 872.3070, within the Dental review panel as a Class II device.