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

    N-ASSAY GLU-UL

    K Number: K980883 · Decision Sep 3, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    48
    Registration Numbers
    48
    Same Product Code
    142
    Applicant Total
    29
    Review Days
    178

    Basic Information

    Device Name
    N-ASSAY GLU-UL
    K Number
    K980883
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1345
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    CRESTAT DIAGNOSTICS, INC.
    Date Received
    March 9, 1998
    Decision Date
    September 3, 1998
    Product Code
    CFR
    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
    CFR Hexokinase, Glucose

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