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

    EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS

    K Number: K925186 · Decision Jan 12, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    85
    Registration Numbers
    85
    Same Product Code
    470
    Applicant Total
    3
    Review Days
    90

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    Basic Information

    Device Name
    EQUILIBRIUM RADIONUCLIDE ANGIOCARDIORAPHY ANALYSIS
    K Number
    K925186
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1200
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Strichman Medical Equipment, Inc.
    Date Received
    October 14, 1992
    Decision Date
    January 12, 1993
    Product Code
    KPS
    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
    KPS System, Tomography, Computed, Emission

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