meddevicedb.com FDA Device Reference

TPE DIAMOND POINTS

K832855 Class I Traditional
Decision Date
1983-09-29
Sponsor / Applicant
Shofu Dental Corp.

Technical Specification

510(k) Submission ID K832855
Product Code DZP
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4535
Decision Date 1983-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TPE DIAMOND POINTS received FDA 510(k) clearance under submission number K832855, sponsored by Shofu Dental 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 1983-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code DZP and 21 CFR 872.4535, within the Dental review panel as a Class I device.