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BIO-RAY SDX DIGITAL X-RAY SYSTEM

K060179 Class II Traditional
Decision Date
2006-02-08
Sponsor / Applicant
Sigma Biomedics, Inc.

Technical Specification

510(k) Submission ID K060179
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2006-02-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-RAY SDX DIGITAL X-RAY SYSTEM received FDA 510(k) clearance under submission number K060179, sponsored by Sigma Biomedics, 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 2006-02-08.

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.