meddevicedb.com FDA Device Reference

HYBRID POINTS

K854347 Class I Traditional
Decision Date
1985-12-27
Sponsor / Applicant
Shofu Dental Corp.

Technical Specification

510(k) Submission ID K854347
Product Code DZP
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4535
Decision Date 1985-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HYBRID POINTS received FDA 510(k) clearance under submission number K854347, 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 1985-12-27.

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.