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510(k) Data Aggregation

    K Number
    K182383
    Date Cleared
    2019-03-19

    (200 days)

    Product Code
    Regulation Number
    880.6250
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    Non-Sterile, PF Nitrile Examination Gloves, Tested for Use with Chemotherapy Drugs-Blue

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

    A patient examination glove is a disposable device intended for medical purpose that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.

    Device Description

    Non-Sterile, PF Nitrile Examination Gloves, Tested for use with Chemotherapy Drugs - Blue

    AI/ML Overview

    The provided document is a 510(k) clearance letter from the FDA for "Non-Sterile, PF Nitrile Examination Gloves, Tested for Use with Chemotherapy Drugs - Blue." This document does not describe an AI/ML powered device, but rather a standard medical device.

    Therefore, the requested information about acceptance criteria, study details, sample sizes, expert qualifications, adjudication methods, multi-reader multi-case studies, standalone performance, and ground truth for an AI device is not applicable to this document.

    The document does include a table indicating the performance of the gloves with various chemotherapy drugs, specifically the "Average Breakthrough Detection Time." This table could be interpreted as describing device performance against acceptance criteria for chemotherapy drug permeation, but it is not related to AI/ML performance.

    Acceptance Criteria and Reported Device Performance (as related to chemotherapy drug permeation for the gloves):

    Tested Chemotherapy Drug And ConcentrationAcceptance Criteria (Implicit: > 240 minutes where stated otherwise)Reported Device Performance (Average Breakthrough Detection Time)
    Carboplatin, 10 mg/ml(Not explicitly stated, but common industry standard for high resistance)>240 minutes
    Carmustine 3.3 mg/ml(Not explicitly stated)11.3 minutes
    Cisplatin (BCNU), 1.0 mg/ml(Not explicitly stated)> 240 minutes
    Cyclophosphamide (Cytoxan), 20.0 mg/ml(Not explicitly stated)> 240 minutes
    Dacarbazine (DTIC), 10.0 mg/ml(Not explicitly stated)> 240 minutes
    Doxorubicin Hydrochloride, 2.0 mg/ml(Not explicitly stated)> 240 minutes
    Etoposide (Toposar), 20.0 mg/ml(Not explicitly stated)> 240 minutes
    Fluorouracil, 50.0 mg/ml(Not explicitly stated)> 240 minutes
    Ifosfamide , 50.0 mg/ml(Not explicitly stated)> 240 minutes
    Methotrexate, 25 mg/ml(Not explicitly stated)> 240 minutes
    Mitomycin C, 0.5 mg/ml(Not explicitly stated)> 240 minutes
    Mitoxantrone, 2 mg/ml(Not explicitly stated)> 240 minutes
    Paclitaxel (Taxol), 6.0 mg/ml(Not explicitly stated)> 240 minutes
    ThioTEPA (10.0 mg/ml)(Not explicitly stated)7.4 minutes
    Vincristine Sulfate, 1.0 mg/ml(Not explicitly stated)> 240 minutes

    The document states that "Carmustine (3.3 mg/ml): 11.3 minutes" and "ThioTEPA (10.0 mg/ml): 7.4 minutes" have "extremely low permeation time," which implies that for these drugs, the gloves do not offer extended protection. This information would be crucial for users to understand the limitations of the device.

    All other requested information about an AI/ML study is not present in this document as it is not a submission for an AI/ML medical device.

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