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

    ANEUVYSION

    K Number: K972200 · Decision Oct 20, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    2
    Applicant Total
    9
    Review Days
    132

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    Basic Information

    Device Name
    ANEUVYSION
    K Number
    K972200
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.4700
    Medical Specialty
    Immunology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Vysis
    Date Received
    June 10, 1997
    Decision Date
    October 20, 1997
    Product Code
    OYU
    Advisory Committee
    Immunology
    Review Advisory Committee
    PA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    OYU Dna-Probe Kit, Human Chromosome

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    Other Clearances by Vysis

    K Number Device Name
    DEN040010 VYSIS AUTOVYSION SYSTEM
    K033982 MODIFICATION TO VYSIS UROVYSION BLADDER CANCER RECURRENCE TEST
    K013785 UROVYSION BLADDER CANCER RECURRENCE KIT
    K011031 VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT
    K010288 ANEUVYSION MULITICOLOR DNA PROBE KIT
    K954214 CEP X SPECTRUMORANGE\Y SPECTRUMGREEN DNA PROBE KIT
    K962873 CEP 12 SPECTRUMORANGE DIRECT LABELED CHROMOSOME ENUMERATION DNA PROBE
    K953591 CEP 8 SPECTRUMORANGE DNA PROBE KIT