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MICRODOSE RC-EZ

K924825 Class I Traditional
Decision Date
1993-03-05
Sponsor / Applicant
Unicep

Technical Specification

510(k) Submission ID K924825
Product Code EKM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3850
Decision Date 1993-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRODOSE RC-EZ received FDA 510(k) clearance under submission number K924825, sponsored by Unicep. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1993-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code EKM and 21 CFR 872.3850, within the Dental review panel as a Class I device.