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

    QUANTASCOPE

    K Number: K870442 · Decision Aug 11, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    189

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    Basic Information

    Device Name
    QUANTASCOPE
    K Number
    K870442
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2320
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Vital Science Corp.
    Date Received
    February 3, 1987
    Decision Date
    August 11, 1987
    Product Code
    DXR
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DXR Ballistocardiograph

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