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510(k) Data Aggregation

    K Number
    K173197
    Manufacturer
    Date Cleared
    2018-08-21

    (323 days)

    Product Code
    Regulation Number
    870.1120
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The reusable blood pressure cuff is an accessory used in conjunction with noninvasive blood pressure measurement systems. The cuff is non-sterile and may be reused. It is available in neonate, infant, child and adult sizes.

    Device Description

    The device comprises tubing attached to an inelastic sleeve with an integrated inflatable bladder that is wrapped around the patient's limb and secured by hook and loop closure. The device tubing is connected to a non-invasive blood pressure measurement system. The reusable NIBP cuff has 9 models with different size for different population with different arm size.

    AI/ML Overview

    This document is a 510(k) summary for a Reusable NIBP Cuff, not an AI/ML medical device submission. Therefore, it does not contain the information requested in the prompt regarding acceptance criteria and study details for an AI-powered device.

    The document discusses the substantial equivalence of the Reusable NIBP Cuff to an existing predicate device based on:

    • Intended use and Indications for Use: An accessory for non-invasive blood pressure measurement systems, non-sterile, reusable, available in various sizes.
    • Technical specifications: Material, tube number, limb circumference range, repeated inflation limits, pressure limits, sterility, biocompatibility.
    • Performance Data: Non-clinical tests according to ISO 81060-1 (Non-Invasive Sphygmomanometers), ISO 10993-5 (In Vitro cytotoxicity), and ISO 10993-10 (irritation and skin sensitization).
    • Clinical test: Explicitly stated as "not required" for this device.

    None of the requested information regarding AI/ML device performance, acceptance criteria, sample sizes for AI model testing, expert consensus, MRMC studies, or ground truth establishment for AI is present in this regulatory submission for a physical medical device.

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