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

    ACCESS FOLATE ASSAY (MODIFICATION)

    K Number: K955434 · Decision Jan 29, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    39
    Registration Numbers
    39
    Same Product Code
    63
    Applicant Total
    199
    Review Days
    119

    Basic Information

    Device Name
    ACCESS FOLATE ASSAY (MODIFICATION)
    K Number
    K955434
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1295
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    BECKMAN COULTER, INC.
    Date Received
    October 2, 1995
    Decision Date
    January 29, 1996
    Product Code
    CGN
    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
    CGN Acid, Folic, Radioimmunoassay

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