# K052206: Zeus Male Condom Applicator

- Pathway: 510(k) (Abbreviated)
- Applicant: Condax, LLC
- Decided: Sep 12, 2006 after 396 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
Longest line of descent: 2 generations back to K874383 (1988). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031007: Kwikeze Male Condom Applicator, Condax, LLC (2003) Summary page 1.

## Indications for use
The Zeus TM Male Condom Applicator facilitates correct positioning (donning) of a male latex condom prior to sexual intercourse. The condom is used for contraceptive and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted infections).

Source page: https://510kreport.com/device/K052206
Methodology: https://510kreport.com/methodology