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

    MAGNETOM Lumina and MAGNETOM Vida Fit with syngo MR XA50A

    K Number: K220939 · Decision Apr 29, 2022
    View on FDA
    Classifications
    1
    FEI Numbers
    152
    Registration Numbers
    152
    Same Product Code
    1071
    Applicant Total
    16
    Review Days
    29

    Basic Information

    Device Name
    MAGNETOM Lumina and MAGNETOM Vida Fit with syngo MR XA50A
    K Number
    K220939
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.1000
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Siemens Medical Solutions USA Inc.
    Date Received
    March 31, 2022
    Decision Date
    April 29, 2022
    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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