K Number
K013320
Date Cleared
2001-12-19

(75 days)

Product Code
Regulation Number
880.6250
Panel
HO
Reference & Predicate Devices
N/A
Predicate For
N/A
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

Blue Latex Examination Gloves, Powder Free

AI/ML Overview

The provided text is a 510(k) premarket notification approval letter for "Blue Latex Examination Gloves, Powder Free." This document indicates that the device has been found substantially equivalent to legally marketed predicate devices, meaning it meets the necessary standards for safety and effectiveness.

However, the document does not contain the detailed acceptance criteria and study information typically found in a clinical study report or a more comprehensive summary of safety and effectiveness data. It is a regulatory approval letter that references such data but does not provide it in detail.

Therefore, based on the provided text, I cannot answer the questions regarding specific acceptance criteria, reported device performance, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, or training set details. This information would normally be found in the 510(k) submission itself or a summary of its data, not in the approval letter.

The primary function of this document is to inform the manufacturer that their device can be legally marketed.

§ 880.6250 Non-powdered patient examination glove.

(a)
Identification. A non-powdered patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner. A non-powdered patient examination glove does not incorporate powder for purposes other than manufacturing. The final finished glove includes only residual powder from manufacturing.(b)
Classification. Class I (general controls). The device, when it is a finger cot, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 880.9.