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DIGITAL RADIOGRAPHY CXDI-410C WIRELESS

K171270 Class II Traditional
Decision Date
2017-11-17
Sponsor / Applicant
Canon, Inc.

Technical Specification

510(k) Submission ID K171270
Product Code MQB
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2017-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIGITAL RADIOGRAPHY CXDI-410C WIRELESS received FDA 510(k) clearance under submission number K171270, sponsored by Canon, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2017-11-17.

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.