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DXS DIGITAL X-RAY SYSTEM

K013271 Class II Traditional
Decision Date
2001-12-13
Sponsor / Applicant
Douglas C. Yoon, Dds

Technical Specification

510(k) Submission ID K013271
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2001-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DXS DIGITAL X-RAY SYSTEM received FDA 510(k) clearance under submission number K013271, sponsored by Douglas C. Yoon, Dds. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2001-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.