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

    CURITY PERCUTANEOUS CATHETER INSERTION KIT

    K Number: K855061 · Decision Apr 16, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    273
    Registration Numbers
    273
    Same Product Code
    701
    Applicant Total
    63
    Review Days
    119

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    Basic Information

    Device Name
    CURITY PERCUTANEOUS CATHETER INSERTION KIT
    K Number
    K855061
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    The Kendal Co.
    Date Received
    December 18, 1985
    Decision Date
    April 16, 1986
    Product Code
    DYB
    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
    DYB Introducer, Catheter

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