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510(k) Data Aggregation

    K Number
    K022751
    Date Cleared
    2002-11-04

    (77 days)

    Product Code
    Regulation Number
    876.4300
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS

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

    Cold biopsy forceps are intended to be used through an endoscope to remove polyps and/or tissue specimens throughout the alimentary tract

    Hot Biopsy Forceps are intended to be used through an endoscope to cauterize and remove polyps and/or tissue specimens throughout the alimentary tract.

    MDS reprocessed biopsy forceps are disposable unless reprocessed again by MDS.

    Device Description

    MDS intends to market Reprocessed Used Disposable Biopsy Forceps. Reprocessing Biopsy Forceps is performed by MDS to MDS protocol Number 40003.

    "Reprocessed," means all operations performed to render a contaminated single-use device patient ready (Enforcement Priorities for Single-Use Devices Reprocessed by Third Party Reprocessors and Hospitals). MDS is a "third party reprocessor" and reprocesses used, single-use medical devices.

    MDS believes that Used Disposable Biopsy Forceps can be considered "reusable - by MDS" as defined in the Food and Drug Administration Compliance Policy Guide #7124.16: they are able to withstand the necessary cleaning and sterilization process, the physical characteristics or quality of the device will not be adversely effected, and the device remains safe and effective for its intended use.

    Biopsy forceps are long instruments with a small jaw type mechanism on one end and a handle mechanism on the other. Forceps are designed to collect tissue samples.

    AI/ML Overview

    The provided text is a 510(k) summary and FDA clearance letter for a reprocessed medical device (biopsy forceps). It does not contain information about studies related to AI/algorithm performance. Therefore, I cannot generate an answer that includes details about acceptance criteria, device performance, sample sizes, ground truth establishment, expert qualifications, adjudication methods, MRMC studies, or standalone algorithm performance for AI-based devices.

    The document discusses the substantial equivalence of the reprocessed physical device to legally marketed predicate devices, focusing on the ability of the physical device to withstand reprocessing and remain safe and effective for its intended use. There is no mention of any AI or algorithmic component in the reprocessed biopsy forceps.

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