# K990710: Barrierplus Synthetic Powder-Free Surgical Gloves

- Pathway: 510(k) (Traditional)
- Applicant: Barriermed Glove Co.
- Decided: May 20, 1999 after 77 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K050181: Medigloves Sterile Powder-Free Synthetic Polyisoprene Surgical Gloves (2005), 0 descendants of its own
- K022873: Powder-Free Radiation Attenuating Neoprene Surgical Glove (Black) (2003), 0 descendants of its own

## Indications for use
These gloves are intended for use in sterile environments within hospitals and other healthcare facilities. The gloves are appropriate for use during invasive surgical procedures as well as non-invasive activities requiring sterility. They are designed to be worn by operating room personnel to protect a surgical wound from contamination and to protect the user from blood-borne pathogens.

Source page: https://510kreport.com/device/K990710
Methodology: https://510kreport.com/methodology