K Number
K990878
Date Cleared
1999-05-21

(66 days)

Product Code
Regulation Number
880.6250
Reference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

Brightway™ Brand Colored Nitrile Examination Glove (Powder Free is a disposable patient examination glove which is worn on the hand o healthcare and similar personnel to prevent contamination between patient and examiner.

Device Description

Brightway™ Brand Colored Nitrile Examination Gloves (Powder Free)

AI/ML Overview

The provided text is a 510(k) premarket notification letter from the FDA regarding "Brightway™ Brand Blue Nitrile Examination Gloves Powder-Free". This document does not contain information about acceptance criteria or a study proving that a device meets acceptance criteria.

Instead, it is a regulatory document stating that the FDA has determined the device to be substantially equivalent to devices marketed prior to May 28, 1976. It outlines the general controls provisions of the Act that the manufacturer must adhere to, such as annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.

Therefore, I cannot provide the requested information.

§ 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.