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

    BIO-RAD CLINICAL DATA MANAGEMENT SYSTEM

    K Number: K942451 · Decision Nov 10, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    18
    Applicant Total
    319
    Review Days
    171

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    Basic Information

    Device Name
    BIO-RAD CLINICAL DATA MANAGEMENT SYSTEM
    K Number
    K942451
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2260
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Bio-Rad
    Date Received
    May 23, 1994
    Decision Date
    November 10, 1994
    Product Code
    LDM
    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
    LDM Instrumentation, High Pressure Liquid Chromatography

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