Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K971212
    Manufacturer
    Date Cleared
    1997-05-27

    (55 days)

    Product Code
    Regulation Number
    880.5725
    Reference & Predicate Devices
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    Replacement battery for Abbott Medical Electronics 0810-0077, 140050-080 Enteral Pump Model #076 FlexiFlow II, 510(k) Number K821661.

    This battery is shipped only to customers who request a replacement battery for a particular device or This battery is shipped only to ouslomers with Teques a replacemician therefore knows the intended use is as a replacement battery.

    Device Description

    Rechargeable Battery Part Number GL4018

    AI/ML Overview

    This document is a 510(k) premarket notification letter from the FDA to Alexander Manufacturing Company regarding their rechargeable battery, part number GL4018. It states that the device is substantially equivalent to legally marketed predicate devices.

    Based on the provided text, the document focuses on the FDA's clearance of a replacement battery and does not contain information about acceptance criteria or a study that proves the device meets specific performance criteria in the way typically associated with medical device efficacy studies (e.g., clinical trials or performance testing with specific metrics like sensitivity, specificity, accuracy).

    The "Indications for Use" section simply states: "Replacement battery for Abbott Medical Electronics 0810-0077, 140050-080 Enteral Pump Model #076 FlexiFlow II, 510(k) Number K821661." This indicates that its primary function is to serve as a power source for an existing, cleared medical device.

    Therefore, I cannot provide the requested information because the provided text does not contain details about acceptance criteria or a study that proves the device meets those criteria for performance as a medical diagnostic or therapeutic device. The regulatory approval here is for a component (a battery) based on substantial equivalence, implying it performs functionally similarly to existing cleared batteries for that specific pump.

    If this were a different type of medical device (e.g., an AI-powered diagnostic tool), the document would typically include performance data, study designs, and detailed acceptance criteria for metrics like sensitivity, specificity, accuracy, etc.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1