# K083752: Gluseal 90, Model GLU9010

- Pathway: 510(k) (Traditional)
- Applicant: Glustitch, Inc.
- Decided: Feb 23, 2009 after 68 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: 4 generations back to K002338 (2001). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063202: Proderma Liquid Bandage, Procurement Technology Systems, LLC (2007) Summary page 1.
- K002338: Liquiderm Liquid Adhesive Bandage, Closure Medical Corp. (2001)

## Indications for use
GluSeal® 90 liquid adhesive bandage is intended to cover minor cuts, scrapes, bums, and minor irritations of the skin and help protect them from infection.

Source page: https://510kreport.com/device/K083752
Methodology: https://510kreport.com/methodology