meddevicedb.com FDA Device Reference

LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS

K905542 Class I Traditional
Decision Date
1991-03-11
Sponsor / Applicant
Lares Research, Inc.

Technical Specification

510(k) Submission ID K905542
Product Code EFB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 1991-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LARES APOLLO CS AND S HANDPIECE LIGHTING SYSTEMS received FDA 510(k) clearance under submission number K905542, sponsored by Lares Research, 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 1991-03-11.

Classification & Regulation

This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.