BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    DIA-KART

    K Number: K841180 · Decision Mar 20, 1984
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    —

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    Basic Information

    Device Name
    DIA-KART
    K Number
    K841180
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    Micro Encapsulation Tech.
    Date Received
    March 20, 1984
    Decision Date
    March 20, 1984
    Advisory Committee
    Unknown
    Review Advisory Committee
    GU
    Third Party
    N

    Other Clearances by Micro Encapsulation Tech.

    K Number Device Name
    K841178 ALU-KART
    K841179 HEMO-KART