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

    AUTOLOGOUS BLOOD PROCESSING SYSTEM

    K Number: K913181 · Decision May 20, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    53
    Registration Numbers
    53
    Same Product Code
    194
    Applicant Total
    23
    Review Days
    307

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    Basic Information

    Device Name
    AUTOLOGOUS BLOOD PROCESSING SYSTEM
    K Number
    K913181
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5830
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Lifestream Int'L, Inc.
    Date Received
    July 18, 1991
    Decision Date
    May 20, 1992
    Product Code
    CAC
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    CAC Apparatus, Autotransfusion

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