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

    PIPETTE, DILUTING, MODEL ADP-30SD

    K Number: K770773 · Decision Jul 11, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    72
    Registration Numbers
    72
    Same Product Code
    139
    Applicant Total
    56
    Review Days
    74

    Basic Information

    Device Name
    PIPETTE, DILUTING, MODEL ADP-30SD
    K Number
    K770773
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2750
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    G.D. SEARLE AND CO.
    Date Received
    April 28, 1977
    Decision Date
    July 11, 1977
    Product Code
    JQW
    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
    JQW Station, Pipetting And Diluting, For Clinical Use

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