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

    GLUCOSITE TEST SYSTEM

    K Number: K971145 · Decision Sep 17, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    131
    Registration Numbers
    131
    Same Product Code
    400
    Applicant Total
    7
    Review Days
    173

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    Basic Information

    Device Name
    GLUCOSITE TEST SYSTEM
    K Number
    K971145
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1345
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Gds Technology, LLC
    Date Received
    March 28, 1997
    Decision Date
    September 17, 1997
    Product Code
    CGA
    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
    CGA Glucose Oxidase, Glucose

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    Other Clearances by Gds Technology, LLC

    K Number Device Name
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    K911801 KETOSITE(TM)/STAT-SITE(TM)/KETOSITE(TM) LOW-HI CON
    K882038 GDS ENZYMATIC SALICYLATE REAGENT
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