# K073663: Gelspray Wound Dressing

- Pathway: 510(k) (Traditional)
- Applicant: Biocure, Inc.
- Decided: Jan 30, 2008 after 35 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 K002338 (2001). 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)
- K053409: 3M Liquid Bandage, 3M Company (2006) Summary page 1.
- K062602: Band-Aid (R) Brand Liquid Bandage, Johnson & Johnson Consumer Companies, Inc. (2006) Summary page 1.

## Indications for use
GelSpray TM Liquid Bandage is indicated for use to cover minor cuts, scrapes and minor irritations of the skin.

Source page: https://510kreport.com/device/K073663
Methodology: https://510kreport.com/methodology