# K955103: 3M NO Sting Barrier Film

- Pathway: 510(k) (Traditional)
- Applicant: 3M Medical Products Group
- Decided: Feb 5, 1996 after 89 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.
8 later devices descend from it; 5 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023163: Liquishield-S (0.7G), Model LS 0010, Liquishield-S (2.0G), Model LS 0020 (2003), 2 descendants of its own
- K083087: Ecocel (2009), 1 descendant of its own
- K980117: Nuvo Barrier Film (1998), 1 descendant of its own
- K153571: Cavilon Advanced High Endurance Skin Protectant (2016), 0 descendants of its own
- K160684: Atteris No-Sting Skin Protectant (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K955103
Methodology: https://510kreport.com/methodology