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

    NEEDLES, STERILE, AIRWAY

    K Number: K770425 · Decision Apr 15, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    466
    Registration Numbers
    466
    Same Product Code
    680
    Applicant Total
    6
    Review Days
    39

    Basic Information

    Device Name
    NEEDLES, STERILE, AIRWAY
    K Number
    K770425
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5570
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    PFIZER PHARMACEUTICALS
    Date Received
    March 7, 1977
    Decision Date
    April 15, 1977
    Product Code
    FMI
    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
    FMI Needle, Hypodermic, Single Lumen

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