K Number
K022639
Date Cleared
2002-09-16

(39 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 purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner.

Device Description

Synthetic Powder Free Vinyl Patient Exam Gloves

AI/ML Overview

The provided text is a 510(k) clearance letter from the FDA for a device described as "Synthetic Powdered Free Vinyl Examination Glove." This document does not contain information about acceptance criteria, device performance, sample sizes, ground truth establishment, or any study details as typically associated with performance testing for AI/ML devices or complex medical devices.

The letter is a regulatory notification of substantial equivalence to a predicate device, which primarily concerns the classification and marketability of the device, subject to general controls. It confirms that the device is a Class I medical device (Patient Examination Gloves) and is substantially equivalent to legally marketed predicate devices.

Therefore, I cannot provide the requested information based on the input text. The information requested (acceptance criteria table, sample sizes, expert qualifications, adjudication methods, MRMC studies, standalone performance, ground truth types, training set details) is typically found in a 510(k) summary, clinical study reports, or performance testing documentation, none of which are present in this FDA clearance letter.

§ 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.