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510(k) Data Aggregation

    K Number
    K003748
    Device Name
    TIANXIE
    Date Cleared
    2001-01-26

    (53 days)

    Product Code
    Regulation Number
    880.5580
    Why did this record match?
    Applicant Name (Manufacturer) :

    SUZHOU TIANYI ACUPUNCTURE INSTRUMENTS CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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