BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    CLP ELEVATED LIPID CONTROL

    K Number: K895858 · Decision Jan 26, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    169
    Registration Numbers
    169
    Same Product Code
    1953
    Applicant Total
    27
    Review Days
    115

    Basic Information

    Device Name
    CLP ELEVATED LIPID CONTROL
    K Number
    K895858
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6250
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    CREATIVE LABORATORY PRODUCTS, INC.
    Date Received
    October 3, 1989
    Decision Date
    January 26, 1990
    Product Code
    LYY
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LYY Latex Patient Examination Glove

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    Other Clearances by CREATIVE LABORATORY PRODUCTS, INC.

    K Number Device Name
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    K922995 LIPID CONTROLS
    K913427 SICKLE HEMOGLOBIN (HBA/S) CONTROL SET
    K913371 TOTAL IRON AND UNSAT IRON BIND CAPAC/IRON BIND CAL
    K913585 LIPASE LINEARITY CONTROL
    K913224 LIPID LINEARITY CONTROLS
    K913496 CHOLINESTERASE LINEARITY CONTROL
    K912823 HIGH DENSITY LIPOPROTEIN CHOLESTEROL
    K912725 TOTAL IRON & UNSAT IRON BIND CAP/IRON BIND CONTROL
    Search all 27 clearances from CREATIVE LABORATORY PRODUCTS, INC. →