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

    19091-XXXXX SER. OF GLASS CAPILLARY COL.

    K Number: K791893 · Decision Oct 30, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    4
    Applicant Total
    230
    Review Days
    35

    Basic Information

    Device Name
    19091-XXXXX SER. OF GLASS CAPILLARY COL.
    K Number
    K791893
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2250
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    HEWLETT-PACKARD CO.
    Date Received
    September 25, 1979
    Decision Date
    October 30, 1979
    Product Code
    DII
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    TX
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    DII Columns, Glc

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