# K083531: Liquiband Ultima, Model LB0004

- Pathway: 510(k) (Traditional)
- Applicant: Medlogic Global, Ltd.
- Decided: Feb 12, 2009 after 76 days
- Product code: MPN (Tissue Adhesive For The Topical Approximation Of Skin)
- Device class: 2
- Regulation: 21 CFR 878.4010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to P010002 (2002). 1 ancestor in all.
10 later devices descend from it; 2 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- P010002: Indermil (TM) Tissue Adhesive, Covidien Lp, Formerly Registered AS United States (2002) Summary page 1.

## Most influential descendants
- K100284: Liquiband Ultima, Lut 003 (2010), 9 descendants of its own
- K110184: Liquiband Flow Control (2011), 6 descendants of its own
- K122446: Liquidband Flow Control (2012), 5 descendants of its own
- K123133: Barle Tissue Adhesive (2013), 3 descendants of its own
- K132243: Barle Tissue Adhesive 2 (2013), 2 descendants of its own

## Indications for use
LiquiBand® Topical Skin Adhesive is indicated for the closure of topical skin incisions including laparoscopic incisions, and trauma-induced lacerations in areas of low skin tension that are simple, thoroughly cleansed, and have easily approximated edges. LiquiBand Topical Skin Adhesive may be used in conjunction with, but not in place of, deep dermal stitches.

Source page: https://510kreport.com/device/K083531
Methodology: https://510kreport.com/methodology