CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C— 510(k) K031633

Name: FDA 510(k) clearance K031633
Creator: U.S. Food and Drug Administration
Published: 2003-06-11

Substantially Equivalent

Canon USA, Inc.

FDA 510(k) clearance K031633 for CANON INC., DIGITAL RADIOGRAPHY, MODEL CXDI-40C, Substantially Equivalent on 2003-06-11. Applicant: Canon USA, Inc.. Device class: 2.

Clearance details

Applicant: Canon USA, Inc.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2003-05-27
Decision date: 2003-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Success, NY, US

Download summary PDF View on FDA.gov ↗

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