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YOUNG PROPHY SYSTEM, PS UNIT

K903284 Class II Traditional
Decision Date
1990-12-17
Sponsor / Applicant
Young Dental Manufacturing Co. 1, LLC

Technical Specification

510(k) Submission ID K903284
Product Code KOJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6080
Decision Date 1990-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

YOUNG PROPHY SYSTEM, PS UNIT received FDA 510(k) clearance under submission number K903284, sponsored by Young Dental Manufacturing Co. 1, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1990-12-17.

Classification & Regulation

This clearance is catalogued under FDA product code KOJ and 21 CFR 872.6080, within the Dental review panel as a Class II device.