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KERR PORCELAIN REPAIR PRIMER

K843023 Class II Traditional
Decision Date
1984-10-25
Sponsor / Applicant
Kerr Corporation (Danbury)

Technical Specification

510(k) Submission ID K843023
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1984-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KERR PORCELAIN REPAIR PRIMER received FDA 510(k) clearance under submission number K843023, sponsored by Kerr Corporation (Danbury). The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1984-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.