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EXAFLEX IMPRESSION MATERIAL (MODIFICATION)

K955932 Class II Traditional
Decision Date
1996-03-11
Sponsor / Applicant
GC America, Inc.

Technical Specification

510(k) Submission ID K955932
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 1996-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXAFLEX IMPRESSION MATERIAL (MODIFICATION) received FDA 510(k) clearance under submission number K955932, sponsored by GC America, 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 1996-03-11.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.