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510(k) Data Aggregation

    K Number
    K964403
    Date Cleared
    1997-01-13

    (70 days)

    Product Code
    Regulation Number
    884.5160
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    SIMPLICITY TM ELECTRIC/BATTERY BREAST PUMP KIT (1068)

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

    The powered Simplicity Breast Pump is designed to express milk from the breast.

    Device Description

    The Simplicity Breast Pump uses a mechanical pumping system to generate suction. It is powered either by two (2) standard C batteries (not included with kit) or powered electrically by utilizing the AC adapter which is provided in the kit and can be plugged into any standard wall outlet. The powered motor activates movement of a rubber dlaphragm inside a pumping chamber which provides suction to express breast milk.

    AI/ML Overview

    This document describes the premarket notification (510(k)) for the Simplicity Electric/Battery Breast Pump Kit. It seeks to demonstrate substantial equivalence to a predicate device, the Evenflo Sof-Touch Ultra Breast Pump.

    Here's a breakdown of the requested information based on the provided text:

    1. Table of Acceptance Criteria and Reported Device Performance

    The document doesn't explicitly state "acceptance criteria" with numerical thresholds in the typical sense of a target performance metric. Instead, the acceptance criterion for the Simplicity Breast Pump was to demonstrate substantial equivalence to the Predicate device (Evenflo Sof-Touch Ultra Breast Pump) in terms of vacuum pressure as a function of time.

    Acceptance Criteria (Stated Goal)Reported Device Performance
    Demonstrate substantial equivalence to the predicate device in terms of vacuum pressure as a function of time."The test data demonstrates that the performance of the Simplicity Breast Pump in terms of vacuum pressure as a function of time is suitable for its intended use, and the device is substantially equivalent to the Predicate (Evenflo)."

    2. Sample Size Used for the Test Set and Data Provenance

    The document states, "Laboratory bench testing was performed to assess the effects of the new characteristics of the proposed Simplicity Breast Pump. These tests compared the proposed Simplicity Breast Pump against the Predicate [Evenflo]."

    • Sample Size for the test set: Not specified. The document only mentions "relatively simple experimental methods for determination of vacuum pressures as a function of time" and "laboratory bench testing." It does not provide the number of devices tested or the number of measurements taken.
    • Data Provenance: The testing was "Laboratory bench testing," implying it was conducted in a controlled environment by the manufacturer or a designated facility. The country of origin is not explicitly stated for the testing, but the submitter, The First Years, Inc., is based in Avon, MA, USA. The data is prospective in the sense that it was generated specifically for this 510(k) submission to demonstrate equivalence.

    3. Number of Experts Used to Establish the Ground Truth for the Test Set and Their Qualifications

    Not applicable. This was a bench test evaluating physical performance characteristics (vacuum pressure), not a human-interpreted diagnostic outcome. Therefore, there was no "ground truth" established by human experts in the medical sense. The "ground truth" or reference was the performance of the predicate device.

    4. Adjudication Method for the Test Set

    Not applicable. As this was a bench test comparing a physical property (vacuum pressure), there was no human adjudication of diagnostic outcomes. The comparison was based on objective measurements.

    5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study Was Done

    No, a Multi-Reader Multi-Case (MRMC) comparative effectiveness study was not done. This study focused on the physical performance characteristics of a breast pump, not the diagnostic efficacy or interpretation by human readers.

    6. If a Standalone (i.e., algorithm only without human-in-the-loop performance) Was Done

    This is not applicable in the context of a breast pump. There is no "algorithm" in the sense of AI or a diagnostic tool that would have a standalone performance. The "device" itself is a mechanical and electrical system whose performance was evaluated in isolation (standalone) from a user, by measuring its physical output.

    7. The Type of Ground Truth Used

    The "ground truth" for the comparison was the performance of the predicate device (Evenflo Sof-Touch Ultra Breast Pump) in terms of vacuum pressure as a function of time. This is a form of empirical data from an established, legally marketed device used as a benchmark for substantial equivalence.

    8. The Sample Size for the Training Set

    Not applicable. This device is a mechanical breast pump, not an AI or machine learning algorithm that requires a "training set."

    9. How the Ground Truth for the Training Set Was Established

    Not applicable, as there is no training set for this type of device.

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