# K232470: Polyisoprene Extra Large Condom

- Pathway: 510(k) (Abbreviated)
- Applicant: Suretex Limited
- Decided: May 9, 2024 after 267 days
- Product code: MOL (Condom, Synthetic)
- 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
Longest line of descent: 3 generations back to K941258 (1995). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K160399: Skyn Original Polyisoprene Lubricated Male Condom, Ansell Healthcare Products, LLC (2016) Summary page 5.

## Indications for use
Polyisoprene Extra Large Condoms are used for contraception and for prophylactic purposes to help reduce the risk of pregnancy and the transmission of sexually transmitted infections (STIs).

Source page: https://510kreport.com/device/K232470
Methodology: https://510kreport.com/methodology