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510(k) Data Aggregation

    K Number
    K981966
    Device Name
    NOSEBLEED NOSECLIP
    Manufacturer
    MICHAEL M. KNOTT, M.D.
    Date Cleared
    1998-08-14

    (71 days)

    Product Code
    EMX
    Regulation Number
    874.4100
    Why did this record match?
    Applicant Name (Manufacturer) :

    MICHAEL M. KNOTT, M.D.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The treatment of simple anterior (front) nosebleeds by application of a noseclip to the external nose in adults and children. Not for use on infants.
    Device Description
    Existing respiratory noseclip is to be used to treat simple anterior (front) nosebleeds.
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    K Number
    K971354
    Device Name
    KNOTT NG TUBE
    Manufacturer
    MICHAEL M. KNOTT, M.D.
    Date Cleared
    1997-11-19

    (222 days)

    Product Code
    FEG
    Regulation Number
    876.5980
    Why did this record match?
    Applicant Name (Manufacturer) :

    MICHAEL M. KNOTT, M.D.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    To permit withdrawal, introduction of fluids into the stomach or removal of stomach gas via a tube inserted through the nostril.
    Device Description
    The Knott NG tube is designed to permit withdrawal or introduction of fluids through a tube which is inserted through the nostril and into the stomach.
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