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

    G+ SYSTEM

    K Number: K101344 · Decision Jun 28, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    34
    Registration Numbers
    34
    Same Product Code
    54
    Applicant Total
    1
    Review Days
    46

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    Basic Information

    Device Name
    G+ SYSTEM
    K Number
    K101344
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    868.1890
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Glytec, LLC (Formally Known AS Glucotec, Inc.)
    Date Received
    May 13, 2010
    Decision Date
    June 28, 2010
    Product Code
    NDC
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    NDC Calculator, Drug Dose

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