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

    MED-PEN/MED-POINT

    K Number: K853733 · Decision Dec 4, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    131
    Registration Numbers
    131
    Same Product Code
    400
    Applicant Total
    2
    Review Days
    454

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    Basic Information

    Device Name
    MED-PEN/MED-POINT
    K Number
    K853733
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1345
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Garid, Inc.
    Date Received
    September 6, 1985
    Decision Date
    December 4, 1986
    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 Garid, Inc.

    K Number Device Name
    K872049 NOVOCHECK/CHECKPOINT/CONTROL SOLUTION