meddevicedb.com FDA Device Reference

VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2

K991239 Class II Traditional
Decision Date
1999-10-18
Sponsor / Applicant
Micron Corp.

Technical Specification

510(k) Submission ID K991239
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 1999-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 received FDA 510(k) clearance under submission number K991239, sponsored by Micron 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 1999-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code ELC and 21 CFR 872.4850, within the Dental review panel as a Class II device.