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

    Roche Digital Pathology Dx

    K Number: K242783 · Decision Dec 17, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    18
    Applicant Total
    48
    Review Days
    92

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    Basic Information

    Device Name
    Roche Digital Pathology Dx
    K Number
    K242783
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    864.3700
    Medical Specialty
    Pathology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ventana Medical Systems, Inc.
    Date Received
    September 16, 2024
    Decision Date
    December 17, 2024
    Product Code
    PSY
    Advisory Committee
    Pathology
    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
    PSY Whole Slide Imaging System

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