# K874383: Mentor Plus (Condom)

- Pathway: 510(k) (Traditional)
- Applicant: Arcon Corp.
- Decided: Mar 7, 1988 after 133 days
- Product code: HIS (Condom)
- Device class: 2
- Regulation: 21 CFR 884.5300
- Recalls of this device: 1 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K031007: Kwikeze Male Condom Applicator (2003), 1 descendant of its own
- K052206: Zeus Male Condom Applicator (2006), 0 descendants of its own

## Recalls of this device
- Dec 26, 2025 · Class II · Z-1181-2026: Potential exposure of rodents and rodent activity in the distribution center.

Source page: https://510kreport.com/device/K874383
Methodology: https://510kreport.com/methodology