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510(k) Data Aggregation

    K Number
    K001295
    Device Name
    PIPER
    Manufacturer
    RTEK MEDICAL SYSTEMS, LLC.
    Date Cleared
    2000-10-25

    (184 days)

    Product Code
    MUJ
    Regulation Number
    892.5050
    Why did this record match?
    Applicant Name (Manufacturer) :

    RTEK MEDICAL SYSTEMS, LLC.

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