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

    MEDI-TECH BALLOON DILATATION CATHETER

    K Number: K910995 · Decision Apr 9, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    92
    Registration Numbers
    92
    Same Product Code
    402
    Applicant Total
    432
    Review Days
    39

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    Basic Information

    Device Name
    MEDI-TECH BALLOON DILATATION CATHETER
    K Number
    K910995
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Boston Scientific Corp
    Date Received
    March 1, 1991
    Decision Date
    April 9, 1991
    Product Code
    LIT
    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
    LIT Catheter, Angioplasty, Peripheral, Transluminal

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