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510(k) Data Aggregation

    K Number
    K160123
    Device Name
    Apinator
    Date Cleared
    2016-07-12

    (174 days)

    Product Code
    Regulation Number
    872.5570
    Why did this record match?
    Applicant Name (Manufacturer) :

    Allen J. Moses, DDS LTD

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The Apinator appliance is intended for use on adult patients 18 years of age and older as an aid for the reduction and /or alleviation of snoring and mild to moderate obstructive sleep apnea.
    Device Description
    Not Found
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