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

    LIQUILYME BUN REAGENT

    K Number: K812945 · Decision Nov 6, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    4
    Registration Numbers
    4
    Same Product Code
    5
    Applicant Total
    39
    Review Days
    17

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    Basic Information

    Device Name
    LIQUILYME BUN REAGENT
    K Number
    K812945
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1770
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Amresco, Inc.
    Date Received
    October 20, 1981
    Decision Date
    November 6, 1981
    Product Code
    LFP
    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
    LFP Conductivity Rate, Urea Nitrogen

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    Other Clearances by Amresco, Inc.

    K Number Device Name
    K905618 GGT REAGENT
    K904468 DIRECT BILIRUBIN REAGENT, 7776/7777/7576/7476/7176
    K905684 ALKALINE PHOSPHATASE
    K905544 MAGNESIUM REAGENT
    K905284 HDL-CHOLESTEROL PRECIPITANT 7773/7573/7473/7173
    K904004 AMRESCOCREAT KINASE REAGENT 7716/17,7516,7416,7116
    K905096 GGT REAGENTS, 7738, 7739, 7538, 7438 & 7138
    K904381 DIAZO COLORIMENTRY DIRECT BILIRUBIN
    K903775 CREATINE PHOSPHOKINASE
    K903829 AST REAGENT
    Search all 39 clearances from Amresco, Inc. →