# K023163: Liquishield-S (0.7G), Model LS 0010, Liquishield-S (2.0G), Model LS 0020

- Pathway: 510(k) (Traditional)
- Applicant: Medlogic Global Limited
- Decided: Jan 13, 2003 after 112 days
- Product code: KMF (Bandage, Liquid)
- Device class: 1
- Regulation: 21 CFR 880.5090
- 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 K955103 (1996). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955103: 3M NO Sting Barrier Film, 3M Medical Products Group (1996) Summary page 1.

## Most influential descendants
- K083087: Ecocel (2009), 1 descendant of its own
- K120059: Liquid Bandage (2012), 0 descendants of its own

## Indications for use
LiquiShield-S is intended to protect intact or damaged skin from the effects of moisture, friction (rubbing), or shear (tearing). LiquiShield-S helps protect skin exposed to irritation from moisture such as urine, faeces, digestive juices, perspiration and wound drainage. LiquiShield-S can also be used in areas that are exposed to friction and shear such as occurs when items, such as bedding, clothing, or shoes, rub against the skin. LiquiShield-S helps protect the skin against irritation caused by adhesive products

Source page: https://510kreport.com/device/K023163
Methodology: https://510kreport.com/methodology