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

    MATERIAL ADDITION LEXAN & K-RESIN

    K Number: K833554 · Decision Mar 12, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    210
    Registration Numbers
    211
    Same Product Code
    499
    Applicant Total
    16
    Review Days
    159

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    Basic Information

    Device Name
    MATERIAL ADDITION LEXAN & K-RESIN
    K Number
    K833554
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1200
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Procedure Products, Inc.
    Date Received
    October 5, 1983
    Decision Date
    March 12, 1984
    Product Code
    DQO
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DQO Catheter, Intravascular, Diagnostic

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