meddevicedb.com FDA Device Reference

REFLECTIONS

K934881 Class I Traditional
Decision Date
1994-02-01
Sponsor / Applicant
Cdb Corp.

Technical Specification

510(k) Submission ID K934881
Product Code EJF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5410
Decision Date 1994-02-01
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 K934881, 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 1994-02-01.

Classification & Regulation

This clearance is catalogued under FDA product code EJF and 21 CFR 872.5410, within the Dental review panel as a Class I device.