# K030574: Gluseal 5ML Dispenser, 1 ML Dispenser, .2 ML Dispenser

- Pathway: 510(k) (Traditional)
- Applicant: Glustitch, Inc.
- Decided: Aug 21, 2003 after 178 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K020338: Stealthstation with Fluoromerge Software, Medtronic Surgical Navigation Technologies (2002). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Most influential descendants
- K071484: Periacryl 90,80,70,60, MODEL9010, 8020, 7030, 6040 (2007), 1 descendant of its own
- K142130: Oral Bond (2016), 0 descendants of its own

## Indications for use
GluSealTM 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/K030574
Methodology: https://510kreport.com/methodology