# K062602: Band-Aid (R) Brand Liquid Bandage

- Pathway: 510(k) (Traditional)
- Applicant: Johnson & Johnson Consumer Companies, Inc.
- Decided: Dec 11, 2006 after 101 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: 2 generations back to K002338 (2001). 2 ancestors in all.
1 later device descends 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)
- K022645: CURAD, Beiersdorf AG (2002) Summary page 1.
- K002338: Liquiderm Liquid Adhesive Bandage, Closure Medical Corp. (2001) Summary page 1.

## Most influential descendants
- K073663: Gelspray Wound Dressing (2008), 0 descendants of its own

## Indications for use
The intended use of the BAND-AID® brand solvent based Liquid bandage is for providing a covering over minor cuts and scrapes that are clean and dry

Source page: https://510kreport.com/device/K062602
Methodology: https://510kreport.com/methodology