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510(k) Data Aggregation

    K Number
    K110285
    Manufacturer
    Date Cleared
    2011-07-14

    (164 days)

    Product Code
    Regulation Number
    876.5665
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    NEPHROS DSU FILTER, NEPHROS MSU FILTER, NEPHROS SSU FILTER

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

    The DSU, MSU, SSU Filters are intended to be used to filter water or bicarbonate concentrate used in hemodialysis devices. The DSU, MSU, SSU Filters assist in providing hemodialysis quality water or bicarbonate concentrate. The device is not a complete water treatment system, but serves to remove biological contaminants. Therefore, it must be used in conjunction with other water treatment equipment (i.e., RO, DI, etc.).

    Device Description

    Not Found

    AI/ML Overview

    The provided text is a 510(k) summary letter from the FDA regarding a medical device called the "Nephros Inc. DSU, MSU, SSU Filter." This document is a regulatory approval letter and an "Indications for Use" statement.

    Based on the content, it's clear that this document concerns a water purification system for hemodialysis and is not an AI/ML medical device. Therefore, the concepts of acceptance criteria, test sets, ground truth, experts, adjudication, MRMC studies, standalone performance, and training sets as typically applied to AI/ML device evaluations are not applicable to this submission.

    The document discusses substantial equivalence to predicate devices, regulatory compliance, and general controls, which are standard for traditional medical devices. There is no information about algorithms, software performance, or diagnostic/prognostic capabilities that would necessitate the metrics and study designs you've asked about.

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