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510(k) Data Aggregation

    K Number
    K970021
    Manufacturer
    Date Cleared
    1997-02-07

    (35 days)

    Product Code
    Regulation Number
    876.5090
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    RUSCH SUPRAPUBIC TRAY

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

    The kit is used for percutaneous bladder drainage and to drain fluids to and from the urinary tract.

    Device Description

    The kit consists of two major components: silicone catheter and plastic introducer assembly, along with attachment tape to fix the catheter to the skin, if required, and an optional scalpel. The kit is used for percutaneous bladder drainage. There are two types of silicone catheters. The first comes equip with one pair of drainage eyes. The second type of silicone catheter comes with six drainage eves arranged in a pigtail shape.

    AI/ML Overview

    This document is a 510(k) Summary for a medical device (Rusch Suprapubic Tray). It describes the device, its intended use, and claims substantial equivalence to legally marketed predicate devices.

    This document does not contain information regarding acceptance criteria, device performance, study details (like sample size, data provenance, ground truth establishment, expert qualifications, adjudication methods, MRMC studies, or standalone algorithm performance).

    Therefore, I cannot fulfill your request for a table of acceptance criteria and reported device performance or other study-related details based on the provided text. The document focuses on regulatory submission for substantial equivalence rather than a detailed performance study.

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