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510(k) Data Aggregation

    K Number
    K020771
    Date Cleared
    2002-05-15

    (68 days)

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

    ACON ONE STEP DRUG SCREEN TEST CARD

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

    The ACON One Step Drug Screen Test Card and ACON One Step Drug Screen Test Card with Integrated Cup are rapid chromatographic immunoassay devices for the qualitative and simultaneous detection of Marijuana, Cocaine, Methamphetamine, Amphetamine, Opiates, Phencyclidine, Benzodiazepine, Methadone, and/or barbiturate in human urine. The test is calibrated using analytes with their respective cutoff concentrations listed in the following table.

    TestCalibratorCut-off
    Amphetamine (AMP)D-Amphetamine1,000 ng/mL
    Barbiturates (BAR)Secobarbital300 ng/mL
    Benzodiazepines (BZO)Oxazepam300 ng/mL
    Cocaine (COC)Benzoylecgonine300 ng/mL
    Methamphetamine (mAMP)D-Methamphetamine1,000 ng/mL
    Morphine (MOP 300 or OPI 300)Morphine300 ng/mL
    Methadone (MTD)Methadone300 ng/mL
    Opiates (OPI 2000)Morphine2,000 ng/mL
    Phencyclidine (PCP)Phencyclidine25 ng/mL
    Marijuana (THC)11-nor- $\Delta^9$ -THC-9 COOH50 ng/mL

    The configurations of the ACON One Step Multi-Drug Screen Test Card and ACON One Step Multi-Drug Screen Test Card with Integrated Cup come with any combination of the above listed drug analytes. They are intended for the healthcare professionals including professionals at point-of-care sites.

    Device Description

    The ACON One Step Drug Screen Test card are competitive binding, lateral flow immunochromatographic assays for the qualitative and simultaneous screening of Marijuana, Cocaine, Methamphetamine, Amphetamine, Opiates, Phencyclidine, Benzodiazepine, Methadone, and/or barbiturate in human urine.

    The test is based on the principle of antigen-antibody immunochemistry. It utilizes mouse monoclonal antibody to selectively detect elevated levels of Marijuana, Cocaine, Methamphetamine. Amphetamine. Opiates. Phencyclidine, Benzodiazepine, Methadone, and/or barbiturate in urine. These tests can be performed without the use of an instrument.

    A drug-positive urine specimen will not generate a colored-line in the designated test region, while a negative urine specimen or a urine specimen containing the drug concentration below the cut-off level will generate a colored-line in the test region. To serve as a procedural control, a colored-line will always appear at the control region, indicating that proper volume of specimen has been applied and membrane wicking has occurred.

    AI/ML Overview

    The provided text describes the ACON One Step Drug Screen Test Card, an immunochromatographic assay for the qualitative and simultaneous detection of various drugs in human urine. The information focuses on the device's intended use and classification but does not contain details about specific acceptance criteria or an analytical study proving that the device meets such criteria.

    Therefore, I cannot fulfill your request for:

    • A table of acceptance criteria and reported device performance.
    • Sample size used for the test set or its data provenance.
    • Number of experts, their qualifications, or adjudication methods for ground truth establishment.
    • Information on a multi-reader multi-case (MRMC) comparative effectiveness study, its effect size, or improvement with AI assistance.
    • Information on a standalone algorithm performance study.
    • The type of ground truth used (beyond implying chemical analysis based on calibrators).
    • Sample size for the training set.
    • How the ground truth for the training set was established.

    The available text primarily serves as a 510(k) summary, detailing the device description, intended use, and regulatory classification for FDA clearance. The key information provided related to performance is the list of analytes and their respective cut-off concentrations, against which the test is calibrated. This implies that the device is intended to accurately detect these drugs at or above these specified cut-off levels.

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