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COMPUTED RADIOGRAPHY SCANNER

K133120 Class II Special
Decision Date
2014-01-15
Sponsor / Applicant
3Disc Americas

Technical Specification

510(k) Submission ID K133120
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2014-01-15
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMPUTED RADIOGRAPHY SCANNER received FDA 510(k) clearance under submission number K133120, sponsored by 3Disc Americas. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-01-15.

Classification & Regulation

This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.