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

    SIREMOBILE 3

    K Number: K827792 · Decision Aug 16, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    781
    Review Days
    19

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    Basic Information

    Device Name
    SIREMOBILE 3
    K Number
    K827792
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Siemens Medical Solutions USA, Inc.
    Date Received
    July 28, 1982
    Decision Date
    August 16, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

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