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HIGH SILVER CONVENTIONAL

K020452 Class II Traditional
Decision Date
2002-05-07
Sponsor / Applicant
Ab Ardent

Technical Specification

510(k) Submission ID K020452
Product Code EJJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3070
Decision Date 2002-05-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIGH SILVER CONVENTIONAL received FDA 510(k) clearance under submission number K020452, sponsored by Ab Ardent. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2002-05-07.

Classification & Regulation

This clearance is catalogued under FDA product code EJJ and 21 CFR 872.3070, within the Dental review panel as a Class II device.