# K031321: Liquishield Liquid Bandage, Model LSB 0001

- Pathway: 510(k) (Traditional)
- Applicant: Medlogic Global Limited
- Decided: Jan 21, 2004 after 271 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 K002338 (2001). 1 ancestor in all.
7 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002338: Liquiderm Liquid Adhesive Bandage, Closure Medical Corp. (2001) Summary page 1.

## Most influential descendants
- K050757: Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional Liquid Bandage (2006), 6 descendants of its own
- K063202: Proderma Liquid Bandage (2007), 5 descendants of its own
- K083913: Chesson Labs Liquid Bandage (2009), 3 descendants of its own
- K131384: Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid Bandage (2014), 2 descendants of its own
- K182733: Rochal Bioshield Silicone Film (2019), 0 descendants of its own

## Indications for use
LiquiShield MT Liquid Bandage is intended to cover minor cuts and scrapes and minor irritations of the skin and help protect them from infection.

Source page: https://510kreport.com/device/K031321
Methodology: https://510kreport.com/methodology