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510(k) Data Aggregation

    K Number
    K010305
    Device Name
    WEISS RETINAL CANNULA
    Manufacturer
    MICRON SURGICAL, INC.
    Date Cleared
    2001-05-02

    (90 days)

    Product Code
    HMX
    Regulation Number
    886.4350
    Why did this record match?
    Applicant Name (Manufacturer) :

    MICRON SURGICAL, INC.

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