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510(k) Data Aggregation

    K Number
    K053035
    Manufacturer
    Date Cleared
    2006-05-05

    (190 days)

    Product Code
    Regulation Number
    862.3250
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    ACRO BIOTECH LLC RAPID BENZOYLECGONINE URINE TEST; CATALOG# MET001000

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

    Acro Rapid Benzoylecgonine (Cocaine) Urine Test is a lateral flow, one-step immunoassay for the qualitative detection of Benzoylecgonine in hyman wipe at a cutoff of 300 ng/mL The test is used to obtain a visual qualitative result and is intended for laboratory use only.

    This assay provides only a preliminary result. Clinical consideration and professional judgment must be applied to a drug test result, particularly in evaluating a preliminary positive result. In order to obtain a confirmed analytical result, a more specific alternate chemical method is needed. Gas Chromatography/ Mass Spectroscopy (GC/MS) anchiate is preferred.

    Device Description

    Acro Rapid Benzoylecgonine (Cocaine) Urine Test is a lateral flow, one-step immunoassay for the qualitative detection of Benzoylecgonine in hyman wipe at a cutoff of 300 ng/mL

    AI/ML Overview

    The provided text is related to the FDA 510(k) premarket notification for the "Acro Rapid Benzoylecgonine (Cocaine) Urine Test." It describes the regulatory approval of the device and its intended use. However, it does not contain any information about acceptance criteria, detailed study results, sample sizes, ground truth establishment, or expert involvement as requested.

    Therefore, I cannot provide a table of acceptance criteria and reported device performance or answer the specific questions regarding the study design and results based on the provided text. The document is a regulatory approval letter and a statement of indications for use, not a detailed study report.

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