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

    ALKALINE PHOSPHATASE MARKER

    K Number: K792548 · Decision Jan 29, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    25
    Applicant Total
    27
    Review Days
    50

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    Basic Information

    Device Name
    ALKALINE PHOSPHATASE MARKER
    K Number
    K792548
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1050
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Electrophoresis Corp. of America
    Date Received
    December 10, 1979
    Decision Date
    January 29, 1980
    Product Code
    CIN
    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
    CIN Electrophoretic Separation, Alkaline Phosphatase Isoenzymes

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    Other Clearances by Electrophoresis Corp. of America

    K Number Device Name
    K802396 GENERAL PROCEDURE AGAROSE FILM
    K792547 AGAROSE BARBITAL BUFFER
    K792551 ALKALINE PHOSPHATASE REAGENT
    K792553 AGAROSE BARBITAL-EDTA BUFFER
    K792574 MOPSO BUFFER
    K792550 PONCEAU S STAIN SET
    K792549 FAT RED 7B STAIN SET
    K792552 AMIDO BLACK 10B STAIN
    K791656 ENZYME STABILIZING REAGENT (ESR)
    K791655 CPK ISOENZYME REAGENT
    Search all 27 clearances from Electrophoresis Corp. of America →