DIGITAL RADIOGRAPHY CXDI-702C Wireless, DIGITAL RADIOGRAPHY CXDI-402C Wireless— 510(k) K192632

Name: FDA 510(k) clearance K192632
Creator: U.S. Food and Drug Administration
Published: 2019-11-07

Substantially Equivalent

Canon, Inc.

FDA 510(k) clearance K192632 for DIGITAL RADIOGRAPHY CXDI-702C Wireless, DIGITAL RADIOGRAPHY CXDI-402C Wireless, Substantially Equivalent on 2019-11-07. Applicant: Canon, Inc.. Device class: 2.

Clearance details

Applicant: Canon, Inc.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2019-09-23
Decision date: 2019-11-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Tokyo, JP

Download summary PDF View on FDA.gov ↗

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