BEUDAMED
    FDA 510(k) Substantially Equivalent 🇬🇧 United Kingdom

    MODIFIED ESCHMANN DILATATION CATHETER

    K Number: K864637 · Decision Jan 6, 1987
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    48

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    Basic Information

    Device Name
    MODIFIED ESCHMANN DILATATION CATHETER
    K Number
    K864637
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Eschmann Bros. & Walsh , Ltd.
    Date Received
    November 19, 1986
    Decision Date
    January 6, 1987
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

    Other Clearances by Eschmann Bros. & Walsh , Ltd.

    K Number Device Name
    K852935 ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411
    K781863 DEVICE, FEMALE INCONTINENCE