meddevicedb.com FDA Device Reference

MICRO 2 SYSTEM

K900785 Class I Traditional
Decision Date
1990-04-16
Sponsor / Applicant
Inodent

Technical Specification

510(k) Submission ID K900785
Product Code EGG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3165
Decision Date 1990-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRO 2 SYSTEM received FDA 510(k) clearance under submission number K900785, sponsored by Inodent. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1990-04-16.

Classification & Regulation

This clearance is catalogued under FDA product code EGG and 21 CFR 872.3165, within the Dental review panel as a Class I device.