Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K051342
    Device Name
    MEDICAL INTERPOROUS
    Manufacturer
    Date Cleared
    2006-06-02

    (375 days)

    Product Code
    Regulation Number
    872.3520
    Why did this record match?
    Applicant Name (Manufacturer) :

    BONYF AG

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Medical Interporous is a soaking treatment for the reduction of odor causing microorganisms on dentures and orthodontic retainers.
    Device Description
    Not Found
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1