# K932521: Powderfree Latex Examination Gloves

- Pathway: 510(k) (Traditional)
- Applicant: Top Glove Sdn. Bhd.
- Decided: Dec 13, 1994 after 567 days
- Product code: LYY (Latex Patient Examination Glove)
- Device class: 1
- Regulation: 21 CFR 880.6250
- 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; 1 cites 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K112988: Powder Free Latex Patient Exam Glove with Protein Labeling Claim (50 Micrograms Per DM Squared or Less of Water Soluble (2011), 1 descendant of its own
- K123757: Powder Free Latex Patient Examination Gloves, with Protein Content Labeling Claim, Natural Color (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K932521
Methodology: https://510kreport.com/methodology