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

    SPACELABS MODEL 90900

    K Number: K894093 · Decision Nov 30, 1989
    View on FDA
    Classifications
    0
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    82
    Applicant Total
    46
    Review Days
    174

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    Basic Information

    Device Name
    SPACELABS MODEL 90900
    K Number
    K894093
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Spacelabs, Inc.
    Date Received
    June 9, 1989
    Decision Date
    November 30, 1989
    Product Code
    LOS
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

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    K912742 ESOPHAGEAL STETHOSCOPE TEMPERATURE PROBE
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