meddevicedb.com FDA Device Reference

MILLENNIUM

K980585 Class I Traditional
Decision Date
1998-10-08
Sponsor / Applicant
Biolase Technology, Inc.

Technical Specification

510(k) Submission ID K980585
Product Code EFB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 1998-10-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILLENNIUM received FDA 510(k) clearance under submission number K980585, sponsored by Biolase Technology, 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 1998-10-08.

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.