# K152948: Medline Anti-Fog Solution

- Pathway: 510(k) (Traditional)
- Applicant: Medline Industries, Inc.
- Decided: Feb 4, 2016 after 121 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K231822: GOLFF Sterile Anti-Fog Solution (2024), 0 descendants of its own

## Indications for use
The anti-fog solution is intended to be used to prevent 'fogging" (caused by condensation) on the lenses of endoscopic/laparoscopic instruments which are likely to fog during use.

Source page: https://510kreport.com/device/K152948
Methodology: https://510kreport.com/methodology