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

    ANGEION IGITAL ANGEFLATOR

    K Number: K921757 · Decision Mar 18, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    64
    Registration Numbers
    64
    Same Product Code
    56
    Applicant Total
    7
    Review Days
    339

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    Basic Information

    Device Name
    ANGEION IGITAL ANGEFLATOR
    K Number
    K921757
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1650
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Angeion Corp.
    Date Received
    April 13, 1992
    Decision Date
    March 18, 1993
    Product Code
    MAV
    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
    MAV Syringe, Balloon Inflation

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    K895580 Y-ADAPTER W/THOUY BORST
    K894446 ANGEION HEMOSTASIS VALVE INTRODUCER
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