Search Filters

Search Results

Found 2 results

510(k) Data Aggregation

    K Number
    K961880
    Date Cleared
    1996-07-19

    (65 days)

    Product Code
    Regulation Number
    880.6740
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    MEDCARE SUCTION CONNECTING TUBING

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

    The MedCare Suction Connecting Tubing is a single use disposable device indicated for general suction procedures as a connecting conduit from a suction device (i.e. Y ankauer suction device, suction catheter, etc.) to a suction collection canister (vacuum source).

    Device Description

    The MedCare Suction Connecting Tubing is a single use disposable device indicated for general suction procedures as a connecting conduit from a suction device (i.e. Yankauer suction device, suction catheter, etc.) to a suction collection canister (vacuum source). The Suction Connecting Tubing is constructed of polyvinyl chloride (PVC) plastic extruded tubing with injection molded tapered connectors solvent bonded to each end. The connectors and made of PVC and have tapered internal diameters with internal ribs

    AI/ML Overview

    This is a 510(k) summary for a Suction Connecting Tubing device. It describes the device, its intended use, and identifies a predicate device. However, this document does NOT contain information regarding acceptance criteria, performance studies, or any of the detailed data points you've requested about AI/algorithm performance.

    The provided text focuses on the regulatory aspects of introducing a physical medical device (suction tubing), not on the validation of an AI or algorithmic medical device. Therefore, I cannot generate the requested table and information based on this input.

    To answer your request, I would need a 510(k) summary (or similar regulatory submission document) for a device that involves an algorithm, AI, or software component whose performance is being evaluated and compared to acceptance criteria.

    Ask a Question

    Ask a specific question about this device

    K Number
    K960218
    Date Cleared
    1996-03-28

    (72 days)

    Product Code
    Regulation Number
    880.6740
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    CONNECTING TUBING

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

    Ask a specific question about this device

    Page 1 of 1