BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    CORDLESS COMPACT MOBILE X-RAY SYSTEM

    K Number: K002685 · Decision Sep 15, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    235
    Applicant Total
    2
    Review Days
    18

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    Basic Information

    Device Name
    CORDLESS COMPACT MOBILE X-RAY SYSTEM
    K Number
    K002685
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    892.1720
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Medison Radiology Systems, Inc.
    Date Received
    August 28, 2000
    Decision Date
    September 15, 2000
    Product Code
    IZL
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    IZL System, X-Ray, Mobile

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