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

    NOVO CEREBROGRAPH

    K Number: K837322 · Decision Apr 21, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    28

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    Basic Information

    Device Name
    NOVO CEREBROGRAPH
    K Number
    K837322
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Novo Diagnostic Systems
    Date Received
    March 24, 1983
    Decision Date
    April 21, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Novo Diagnostic Systems

    K Number Device Name
    K828574 NOVO BMC LAB 22A BONE MINERAL CONTENT DETERMINATION IN THE AXIAL SKELETON