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510(k) Data Aggregation

    K Number
    K970670
    Device Name
    REUSABLE VITRECTOMY PROBE
    Manufacturer
    Date Cleared
    1997-05-06

    (71 days)

    Product Code
    Regulation Number
    886.4150
    Why did this record match?
    Applicant Name (Manufacturer) :

    ALTEX VISION

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K970673
    Device Name
    DISPOSABLE VITRECTOMY PROBE
    Manufacturer
    Date Cleared
    1997-05-05

    (70 days)

    Product Code
    Regulation Number
    886.4150
    Why did this record match?
    Applicant Name (Manufacturer) :

    ALTEX VISION

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
    Ask a Question

    Ask a specific question about this device

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