meddevicedb.com FDA Device Reference

HYDROCOLOR 5

K102739 Class II Traditional
Decision Date
2010-12-08
Sponsor / Applicant
Cascades Device Consulting Associates

Technical Specification

510(k) Submission ID K102739
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2010-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYDROCOLOR 5 received FDA 510(k) clearance under submission number K102739, sponsored by Cascades Device Consulting Associates. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2010-12-08.

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.