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

    ABL700 SERIES ANALYZER WITH AUTOCHECK MODULE

    K Number: K992859 · Decision Jan 10, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    34
    Registration Numbers
    34
    Same Product Code
    187
    Applicant Total
    50
    Review Days
    138

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    Basic Information

    Device Name
    ABL700 SERIES ANALYZER WITH AUTOCHECK MODULE
    K Number
    K992859
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    862.1120
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Radiometer America, Inc.
    Date Received
    August 25, 1999
    Decision Date
    January 10, 2000
    Product Code
    CHL
    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
    CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

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