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

    UNKNOWN

    K Number: K837513 · Decision Jun 13, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    49

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    Basic Information

    Device Name
    UNKNOWN
    K Number
    K837513
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Xerox Corp.
    Date Received
    April 25, 1983
    Decision Date
    June 13, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Xerox Corp.

    K Number Device Name
    K800164 413A NEONATAL MONITOR