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

    PX-100 PORTABLE X-RAY GENERATOR

    K Number: K921116 · Decision Oct 5, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    77
    Registration Numbers
    77
    Same Product Code
    235
    Applicant Total
    13
    Review Days
    210

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    Basic Information

    Device Name
    PX-100 PORTABLE X-RAY GENERATOR
    K Number
    K921116
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1720
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Acoma Medical Imaging, Inc.
    Date Received
    March 9, 1992
    Decision Date
    October 5, 1992
    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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