XPLORER 2200 DIGITAL RADIOGRAPHIC SYSTEM— 510(k) K063039

Name: FDA 510(k) clearance K063039
Creator: U.S. Food and Drug Administration
Published: 2006-11-02

Substantially Equivalent

Imaging Dynamics Company , Ltd.

FDA 510(k) clearance K063039 for XPLORER 2200 DIGITAL RADIOGRAPHIC SYSTEM, Substantially Equivalent on 2006-11-02. Applicant: Imaging Dynamics Company , Ltd.. Device class: 2.

Clearance details

Applicant: Imaging Dynamics Company , Ltd.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2006-10-03
Decision date: 2006-11-02
Decision: Substantially Equivalent
Clearance type: Special
Location: Calgary, Alberta, CA

Download summary PDF View on FDA.gov ↗

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