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

    CLAMPLESS VALVED CATHETER

    K Number: K962300 · Decision Sep 5, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    90
    Registration Numbers
    90
    Same Product Code
    301
    Applicant Total
    5
    Review Days
    84

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    Basic Information

    Device Name
    CLAMPLESS VALVED CATHETER
    K Number
    K962300
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5970
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bmw Medical, Inc.
    Date Received
    June 13, 1996
    Decision Date
    September 5, 1996
    Product Code
    LJS
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

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    Other Clearances by Bmw Medical, Inc.

    K Number Device Name
    K964439 NEEDLE-FREE VALVED CONNECTOR AND CAP
    K963806 CLAMPLESS VALVED CATHETER - TUNNELED (CVC-T)
    K963215 CLAMPLESS VALVED CATHETER - MIDLINE (CVC-ML)
    K963097 CLAMPLESS VALVED CATHETER-PICC (CVC-PICC)