Digital Radiography CXDI-CS01— 510(k) K222661

Substantially Equivalent

Canon, Inc.

FDA 510(k) clearance K222661 for Digital Radiography CXDI-CS01, Substantially Equivalent on 2022-09-27. 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: 2022-09-02
Decision date: 2022-09-27
Decision: Substantially Equivalent
Clearance type: Special
Location: Kawasaki, JP

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.