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510(k) Data Aggregation

    K Number
    K193263
    Date Cleared
    2020-01-24

    (59 days)

    Product Code
    Regulation Number
    870.1220
    Reference & Predicate Devices
    Why did this record match?
    Reference Devices :

    K030279, K030187

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

    The Reprocessed Achieve Catheter Connecting Cable is designed for use only with the Achieve family of mapping catheters. It is intended to provide connection of the catheter to a standard ECG interface box.

    Device Description

    The Reprocessed Achieve Catheter Connecting Cable provides conduction from the proximal end of the mapping catheter to standard shielded ECG pins that connect standard EP recording and pacing equipment. The cable is designed for use with the Achieve family of mapping catheters.

    AI/ML Overview

    The provided text is a 510(k) summary for the Innovative Health LLC's Reprocessed Achieve Catheter Connecting Cable. This document focuses on demonstrating substantial equivalence to a predicate device, rather than providing a detailed study report of a device's performance against specific acceptance criteria in a clinical or AI-related context.

    Therefore, many of the requested elements for describing "acceptance criteria and the study that proves the device meets the acceptance criteria" are not applicable or not explicitly detailed in this type of FDA submission. This is because the device being described is a reprocessed cable, and the 510(k) emphasizes functional and safety testing to show equivalence to a predicate device, not necessarily a clinical outcomes study with AI components.

    However, I can extract information related to the bench and laboratory testing that was conducted.

    Here's a breakdown of the available information based on your request:

    1. A table of acceptance criteria and the reported device performance

    The document does not explicitly present a table of quantitative acceptance criteria with reported numerical device performance as would be found in a detailed study report. Instead, it lists the types of functional and safety testing performed to ensure the reprocessed device is "as safe and effective as the predicate device."

    Types of Testing Performed:

    • Cleaning Validation
    • Sterilization Validation
    • Functional Testing
      • Visual Inspection
      • Dimensional Verification
      • Electrical Continuity Testing
      • High Potential (HiPOT) Testing
    • Packaging Validation

    The "performance" implied is that the device passed these validations and tests, demonstrating its equivalence. Specific quantitative performance metrics or acceptance thresholds are not provided in this summary. For example, instead of stating "Electrical Continuity: Resistance

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