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DUO DENT

K923694 Class II Traditional
Decision Date
1994-05-18
Sponsor / Applicant
Pdc Management Services, Inc.

Technical Specification

510(k) Submission ID K923694
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 1994-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUO DENT received FDA 510(k) clearance under submission number K923694, sponsored by Pdc Management Services, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1994-05-18.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.