# K063587: Xodus Medical Anti-Fog Solution

- Pathway: 510(k) (Traditional)
- Applicant: Xodus Medical, Inc.
- Decided: Jan 9, 2007 after 39 days
- Product code: OCT (Anti Fog Solution And Accessories, Endoscopy)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K022826 (2002). 1 ancestor in all.
1 later device descends 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)
- K022826: Clear-IT Anti-Fog, Model PS003, Preservation Solutions, Inc. (2002) Summary page 1.

## Most influential descendants
- K111622: Unimax Anti-Fog Solution (2011), 0 descendants of its own

## Indications for use
Anti-Fog is intended to be used to prevent "fogging" caused by condensation on the lenses of endoseopic/laparascopic instruments which are likely to fog during use.

Source page: https://510kreport.com/device/K063587
Methodology: https://510kreport.com/methodology