BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

    GLUCODR SUPERSENSOR SYSTEM

    K Number: K050985 · Decision Oct 7, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    168
    Registration Numbers
    169
    Same Product Code
    507
    Applicant Total
    5
    Review Days
    171

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    Basic Information

    Device Name
    GLUCODR SUPERSENSOR SYSTEM
    K Number
    K050985
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1345
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    All Medicus Co., Ltd.
    Date Received
    April 19, 2005
    Decision Date
    October 7, 2005
    Product Code
    NBW
    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
    NBW System, Test, Blood Glucose, Over The Counter

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