BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    CIBA CORNING ACS:180 AUTOMATED CHEMILUMINESCENCE

    K Number: K902336 · Decision Jun 18, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    174
    Registration Numbers
    174
    Same Product Code
    207
    Applicant Total
    125
    Review Days
    25

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    Basic Information

    Device Name
    CIBA CORNING ACS:180 AUTOMATED CHEMILUMINESCENCE
    K Number
    K902336
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2160
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Ciba Corning Diagnostics Corp.
    Date Received
    May 24, 1990
    Decision Date
    June 18, 1990
    Product Code
    JJE
    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
    JJE Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

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    Other Clearances by Ciba Corning Diagnostics Corp.

    K Number Device Name
    K962559 ACS CORTISOL IMMUNOASSAY
    K963251 CIBA CORNING ACS;180 DPD ASSAY
    K961807 CERTAIN HCT LEVEL A & LEVEL B/CVM HCT LEVELS 1,2,3, & 4
    K961657 CIBA CORNING 400 SYSTEM
    K962021 CIBA CORNING 348 SYSTEM
    K962126 ACS CKMB II IMMUNOASSAY
    K962041 ACS LH2 IMMUNOASSAY
    K961510 ACS FRT4 IMMUNOASSAY
    K960246 LIQUID CARDIAC MARKER 1,2,3 ASSAYED
    K955873 ACS PHENYTOIN ASSAY
    Search all 125 clearances from Ciba Corning Diagnostics Corp. →