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ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS

K903292 Class II Traditional
Decision Date
1990-10-19
Sponsor / Applicant
Coe Laboratories, Inc.

Technical Specification

510(k) Submission ID K903292
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 1990-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS received FDA 510(k) clearance under submission number K903292, sponsored by Coe Laboratories, 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 1990-10-19.

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.