# K002338: Liquiderm Liquid Adhesive Bandage

- Pathway: 510(k) (Traditional)
- Applicant: Closure Medical Corp.
- Decided: Jan 29, 2001 after 181 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
No predicates in its family tree.
23 later devices descend from it; 6 cite it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K022645: CURAD (2002), 16 descendants of its own
- K032948: Elastic Skin Liquid Bandage (2004), 8 descendants of its own
- K042610: DR. Theiss Alergol Pollen Blocker Cream (2005), 7 descendants of its own
- K031321: Liquishield Liquid Bandage, Model LSB 0001 (2004), 7 descendants of its own
- K050757: Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional Liquid Bandage (2006), 6 descendants of its own

Source page: https://510kreport.com/device/K002338
Methodology: https://510kreport.com/methodology