# K872812: Skinless-Skin, Pink Tint (Condom)

- Pathway: 510(k) (Traditional)
- Applicant: Okamoto USA, Inc.
- Decided: Nov 5, 1987 after 112 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K090259: Okamoto Ultra Thin (2009), 3 descendants of its own
- K192669: Extremely Thin 003, ZERO ZERO THREE (2020), 2 descendants of its own
- K252622: Male Latex Condom HA (2026), 0 descendants of its own
- K213921: Microthin Natural Rubber Latex Condom (2022), 0 descendants of its own

Source page: https://510kreport.com/device/K872812
Methodology: https://510kreport.com/methodology