# K002393: Non-Spermicidal Lubricated Male Latex Condom

- Pathway: 510(k) (Abbreviated)
- Applicant: Innolatex Sdn. Bhd
- Decided: Dec 19, 2000 after 134 days
- Product code: HIS (Condom)
- Device class: 2
- Regulation: 21 CFR 884.5300
- 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
- K050244: Male Natural Rubber Latex Condom (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K002393
Methodology: https://510kreport.com/methodology