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

    VAN DELLEN ASPIRATING TUBING

    K Number: K873463 · Decision Nov 23, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    174
    Registration Numbers
    174
    Same Product Code
    23
    Applicant Total
    7
    Review Days
    87

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    Basic Information

    Device Name
    VAN DELLEN ASPIRATING TUBING
    K Number
    K873463
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Van Dellen, Ltd.
    Date Received
    August 28, 1987
    Decision Date
    November 23, 1987
    Product Code
    BYY
    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
    BYY Tube, Aspirating, Flexible, Connecting

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (BYY), ordered by most recent decision date.

    VITAFLOW SUCTION/ASPIRATION TUBING SET

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    CONNECTING TUBING

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    MAXI-FLOW SUCTION HANDLE/THE REEL THING TUBING REEL

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    MAXI-FLOW SUCTION TUBE/TOP GUN SUCTION IRRIGATOR

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    MAXI-FLOW

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    WILTEK IRRIGAITON/ASPIRATION TUBE SET

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    View all

    Other Clearances by Van Dellen, Ltd.

    K Number Device Name
    K873465 VAN DELLEN BACTERIA FILTER
    K873464 VAN DELLEN CANNULA
    K873462 VAN DELLEN ASPIRATOR
    K873162 VAN DELLEN RETROBULBAR NEEDLE
    K873163 VAN DELLEN IRRIGATING CYSTOTOME
    K873164 VAN DELLEN HEALON CANNULA