BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    APO A-I RIA KIT-HUMAN PLASMA APOLIP-

    K Number: K840105 · Decision Jan 10, 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
    APO A-I RIA KIT-HUMAN PLASMA APOLIP-
    K Number
    K840105
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    Iso-Tex Diagnostics
    Date Received
    January 10, 1984
    Decision Date
    January 10, 1984
    Advisory Committee
    Unknown
    Review Advisory Committee
    CH
    Third Party
    N

    Other Clearances by Iso-Tex Diagnostics

    K Number Device Name
    K851389 APO B RIA KIT
    K782081 RIA SYSTEM, PARATHYROID HORMONE