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510(k) Data Aggregation

    K Number
    K992666
    Manufacturer
    Date Cleared
    1999-10-13

    (65 days)

    Product Code
    Regulation Number
    892.2050
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K954159

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Video Plus is a digital imaging acquisition and review system for the cardiac video Fras is a cigation findedigital fluoroscopy, digital fluoroscopy, digital cine, real time cannoterization no. To icatalor meterssing, image processing, quantitative coronary processing digital subtraction angiography, digital video input, linked biplane acquisition, auto injection, and histogram equalization.

    Device Description

    This is a software upgrade for the existing Video Plus System cleared under K954159. This release encompasses some general enhancements and more integrated support for certain vendors.

    AI/ML Overview

    This document is a 510(k) Summary for a software upgrade (Video Plus software upgrade) for an existing digital image acquisition unit, Camtronics Video Plus, cleared under K954159. The submission compares the upgraded device to a predicate device, GE Medical Systems "Advantx DLX" (K945459, K926258).

    The document explicitly states:
    "Performance data: Not required for determination of substantial equivalence for this class of device."
    "Conclusions drawn from clinical and nonclinical test data: Not required for determination of substantial equivalence for this class of device."

    Therefore, the requested information regarding acceptance criteria and a study proving the device meets those criteria cannot be provided from this document as no such data was required or presented for this 510(k) submission. The FDA clearance was based on substantial equivalence to a predicate device, not on specific performance data against acceptance criteria.

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