# K120059: Liquid Bandage

- Pathway: 510(k) (Traditional)
- Applicant: Chesson Laboratory Associates, Inc.
- Decided: May 17, 2012 after 129 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: 3 generations back to K955103 (1996). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083087: Ecocel, Polichem S.A (2009) Summary page 2.

## Indications for use
[The device] is indicated for managing signs and symptoms of nail dystrophy, i.e., nail splitting and nail fragility, for intact or damaged nails. [The device] coats and adheres to the nail surface preventing direct abrasion and friction on the nail surface while also providing protection against the effects of moisture.

Source page: https://510kreport.com/device/K120059
Methodology: https://510kreport.com/methodology