Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K970160
    Date Cleared
    1997-07-15

    (180 days)

    Product Code
    Regulation Number
    878.4460
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    A surgeon's glove is device made of natural or synthetic rubber intended to be worn by the operating room personnel to protect a surgical wound from contamination.

    Device Description

    A surgeon's glove is device made of natural or synthetic rubber intended to be worn by the operating room personnel to protect a surgical wound from contamination.

    AI/ML Overview

    This document is a 510(k) clearance letter from the FDA for Uniject Powdered Latex Surgical Gloves (K970160). It declares the device substantially equivalent to pre-amendment devices. It describes the device's indications for use: "A surgeon's glove is device made of natural or synthetic rubber intended to be worn by the operating room personnel to protect a surgical wound from contamination."

    However, this document does not contain any information regarding acceptance criteria, device performance studies, sample sizes, ground truth establishment, or expert involvement. These details would typically be found in the 510(k) submission itself, not in the clearance letter.

    Therefore, I cannot provide the requested table and information based on the provided text.

    Ask a Question

    Ask a specific question about this device

    Page 1 of 1