BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    POSTERIOR NASAL EPISTAXIS INSTRUMENTS

    K Number: K911756 · Decision Oct 24, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    11
    Applicant Total
    142
    Review Days
    189

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    Basic Information

    Device Name
    POSTERIOR NASAL EPISTAXIS INSTRUMENTS
    K Number
    K911756
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4565
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Richard Wolf Medical Instruments Corp.
    Date Received
    April 18, 1991
    Decision Date
    October 24, 1991
    Product Code
    ECB
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    ECB Unit, Syringe, Air And/Or Water

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