meddevicedb.com FDA Device Reference

PENTRON HIGH STRENGTH PORCELAIN

K864404 Class II Traditional
Decision Date
1986-11-24
Sponsor / Applicant
Pentron Corp.

Technical Specification

510(k) Submission ID K864404
Product Code EIH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6660
Decision Date 1986-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PENTRON HIGH STRENGTH PORCELAIN received FDA 510(k) clearance under submission number K864404, sponsored by Pentron 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 1986-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.