# K131384: Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid Bandage

- Pathway: 510(k) (Traditional)
- Applicant: Kericure, Inc.
- Decided: Aug 7, 2014 after 450 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: 5 generations back to K002338 (2001). 8 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083913: Chesson Labs Liquid Bandage, Chesson Laboratory Associates, Inc. (2009) Summary page 6.
- K991920: Dermaphylyx Hydrophilic Foam Wound Dressing, Dermaphylyx, Inc. (1999) Summary page 6.

## Most influential descendants
- K182733: Rochal Bioshield Silicone Film (2019), 0 descendants of its own
- K171148: Aleo BME Liquid Bandage (2018), 0 descendants of its own

## Indications for use
To help cover and protect the skin from infection in minor cuts, scrapes, burns, irritations and abrasions. To cover and protect the skin from infection in minor cuts, scrapes, burns, irritations and abrasions, as well as closed surgical incisions and excisions.

Source page: https://510kreport.com/device/K131384
Methodology: https://510kreport.com/methodology