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510(k) Data Aggregation

    K Number
    K961055
    Device Name
    CT PROSPEED CT/I
    Manufacturer
    Date Cleared
    1996-06-17

    (91 days)

    Product Code
    Regulation Number
    892.1750
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    CT PROSPEED CT/I

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

    The CT ProSpeed CT/i is indicated for head and whole body xray computed tomography applications. It provides axial, helical and scout imaging.

    Device Description

    The device is an x-ray computed tomography scanner consisting of a gantry, patient table, console, computer, and associated accessories.

    AI/ML Overview

    This document is a 510(k) summary for a CT scanner (CT ProSpeed CT/i). It focuses on demonstrating substantial equivalence to previously marketed devices and ensuring safety. It does not contain information on the acceptance criteria, study design, or performance metrics typically associated with AI/algorithm-driven devices. Therefore, I cannot extract the requested information from the provided text.

    Specifically, the document from 1996 describes a computed tomography (CT) scanner, a hardware device for medical imaging, not an AI or algorithm-driven software device. The acceptance criteria and performance data requested (e.g., sensitivity, specificity, MRMC studies, ground truth establishment) are relevant to software algorithms, particularly those involved in image analysis or diagnosis. These types of studies were not typically performed or reported in 510(k) submissions for hardware imaging devices like CT scanners in 1996.

    Therefore, the requested information cannot be filled from the provided text.

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