meddevicedb.com FDA Device Reference

REFLECTIONS

K973776 Class II Traditional
Decision Date
1997-11-21
Sponsor / Applicant
Cdb Corp.

Technical Specification

510(k) Submission ID K973776
Product Code DYW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 1997-11-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REFLECTIONS received FDA 510(k) clearance under submission number K973776, sponsored by Cdb 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 1997-11-21.

Classification & Regulation

This clearance is catalogued under FDA product code DYW and 21 CFR 872.5470, within the Dental review panel as a Class II device.