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510(k) Data Aggregation

    K Number
    K964891
    Device Name
    ORBSHOT KERATOMETER
    Manufacturer
    ORBTEK, INC.
    Date Cleared
    1997-03-26

    (110 days)

    Product Code
    MMQ
    Regulation Number
    886.1350
    Why did this record match?
    Applicant Name (Manufacturer) :

    ORBTEK, INC.

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