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    FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

    MultiBand SENSE

    K Number: K143606 · Decision May 8, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    146
    Registration Numbers
    146
    Same Product Code
    1098
    Applicant Total
    5
    Review Days
    140

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    Basic Information

    Device Name
    MultiBand SENSE
    K Number
    K143606
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1000
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Philips Medical Systems Nethrlands BV
    Date Received
    December 19, 2014
    Decision Date
    May 8, 2015
    Product Code
    LNH
    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
    LNH System, Nuclear Magnetic Resonance Imaging

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