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

    CLINICAL LABORATORY ANALYZING SYSTEM

    K Number: K041230 · Decision May 20, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    67
    Registration Numbers
    68
    Same Product Code
    72
    Applicant Total
    9
    Review Days
    10

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    Basic Information

    Device Name
    CLINICAL LABORATORY ANALYZING SYSTEM
    K Number
    K041230
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    862.1345
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Hemocue, Inc.
    Date Received
    May 10, 2004
    Decision Date
    May 20, 2004
    Product Code
    LFR
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LFR Glucose Dehydrogenase, Glucose

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    Other Clearances by Hemocue, Inc.

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    K020935 HEMOCUE GLUCOSE 201 SYSTEM, ARTICLE NUMBER 120706
    K962415 HEMOCUE B-GLCOSE SYSTEM
    K961312 HEMOCUE B-HEMOGLOBIN SYSTEM
    K961311 HEMOCUE B-GLUCOSE SYSTEM
    K943432 HEMOCUE B-GLUCOSE SYSTEM
    K911141 HEMOCUE(R) B-GLUCOSE MICROCUVETTE/PHOTOMETER