# K014283: Latex Surgeons Glove (Powder Free)

- Pathway: 510(k) (Traditional)
- Applicant: Brightway Gloves Pvt., Ltd.
- Decided: May 22, 2002 after 146 days
- Product code: KGO (Surgeon'S Gloves)
- Device class: 1
- Regulation: 21 CFR 878.4460
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Class I Surgeon’s Glove (Powder free): named in the summary without a submission number

## Indications for use
Powder free Surgeon’s glove is a sterile powder free medical device intended to be worn by operating room personnel to protect a surgical wound from contamination.

Source page: https://510kreport.com/device/K014283
Methodology: https://510kreport.com/methodology