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

    BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757

    K Number: K020523 · Decision Mar 20, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23
    Same Product Code
    24
    Applicant Total
    15
    Review Days
    29

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    Basic Information

    Device Name
    BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757
    K Number
    K020523
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5570
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bd
    Date Received
    February 19, 2002
    Decision Date
    March 20, 2002
    Product Code
    SCL
    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
    SCL Allergen And Vaccine Delivery Needles

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