# K031263: 3M Liquid Bandage, Model 120-LB

- Pathway: 510(k) (Traditional)
- Applicant: 3M Company
- Decided: Oct 7, 2003 after 169 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.
7 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Johnson & Johnson BAND-AID® Liquid Bandage: named in the summary without a submission number

## Most influential descendants
- K050757: Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional Liquid Bandage (2006), 6 descendants of its own
- K063202: Proderma Liquid Bandage (2007), 5 descendants of its own
- K083913: Chesson Labs Liquid Bandage (2009), 3 descendants of its own
- K131384: Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid Bandage (2014), 2 descendants of its own
- K182733: Rochal Bioshield Silicone Film (2019), 0 descendants of its own

## Indications for use
3MTMLiquid Bandage is intended to cover minor cuts, scrapes, and skin irritations.

Source page: https://510kreport.com/device/K031263
Methodology: https://510kreport.com/methodology