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510(k) Data Aggregation

    K Number
    K022723
    Device Name
    MASTEL 1 FOLDER IMPLANTATION SYSTEM
    Manufacturer
    MASTEL PRECISION, INC.
    Date Cleared
    2002-12-26

    (132 days)

    Product Code
    KYB
    Regulation Number
    886.4300
    Why did this record match?
    Applicant Name (Manufacturer) :

    MASTEL PRECISION, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Mastel 1 Folder™ Implantation System is intended to fold and assist in inserting the SENSAR™, model AR40e intraocular lens, ONLY into the capsular bag.
    Device Description
    The Mastel 1 Folder is an ophthalmic surgical device designed for use in inserting a foldable intraocular lens into the eye. The materials, basic scientific concepts, physical properties and intended use of the Mastel 1 Folder are similar to those of the predicate devices. The Mastel 1 Folder Implantation System is comprised of a medical-grade titanium handpiece, a material commonly used in reusable surgical devices. The handpiece rod is designed to accept a single-use cartridge. The handpiece is reusable and is designed to withstand conventional in-office steam autoclaving. The handpiece is provided to the customer in a plastic case in a non-sterile state.
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