# K003737: Powdered Latex Patient Examination Glove with Protein Content Labeling Claim (200 Microgramsper or Less)

- Pathway: 510(k) (Traditional)
- Applicant: Perusahaan Getah Asas Sdn. Bhd.
- Decided: Feb 1, 2001 after 59 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K120693: Latex Examination Gloves (Powdered) (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K003737
Methodology: https://510kreport.com/methodology