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

    MORSE HEMOSTATIC CATHETER INTRODUCER SET

    K Number: K915078 · Decision Jun 10, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    273
    Registration Numbers
    273
    Same Product Code
    701
    Applicant Total
    28
    Review Days
    215

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    Basic Information

    Device Name
    MORSE HEMOSTATIC CATHETER INTRODUCER SET
    K Number
    K915078
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    North American Instrument Corp.
    Date Received
    November 8, 1991
    Decision Date
    June 10, 1992
    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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