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510(k) Data Aggregation

    K Number
    K021420
    Date Cleared
    2002-06-04

    (32 days)

    Product Code
    Regulation Number
    866.2900
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    PARACON II/FECAL CONCENTRATOR II

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

    ParaCon II / Fecal Concentrator II is a filtration device that is intended for use in the separation of intestinal parasites from: fecal debris in preserved fecal specimens.

    Fecal specimens that have been preserved in preservatives such as formalin, sodium acetate-acetic acid-formalin, merthiolate-formalin, or modified polyvinyl alcohol, and which are contained in 30 ml transport vials, may be mated to the ParaCon II / Fecal Concentrator II filtration device and inverted in order to separate fecal debris from the specimen.

    The filtered specimen may then be concentrated by centrifugation, and observed microscopically.

    Device Description

    ParaCon II / Fecal Concentrator II is a filtration device.

    AI/ML Overview

    The provided text is a 510(k) premarket notification letter from the FDA to Para Scientific, Inc. regarding their ParaCon II / Fecal Concentrator II device. This document is a regulatory approval letter and does not contain the acceptance criteria, study details, or performance data typically found in a scientific study or a detailed technical submission for a medical device.

    Therefore, I cannot provide the requested information. The letter only confirms that the device is substantially equivalent to legally marketed predicate devices and can be marketed based on its stated indications for use. It doesn't include the specific study details that would demonstrate how acceptance criteria were met.

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