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IMPRESSIX, COLORCHANGE ALGINATE

K062400 Class II Traditional
Decision Date
2006-11-16
Sponsor / Applicant
Cavex Holland BV

Technical Specification

510(k) Submission ID K062400
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2006-11-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPRESSIX, COLORCHANGE ALGINATE received FDA 510(k) clearance under submission number K062400, sponsored by Cavex Holland BV. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-11-16.

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.