# KMF: Bandage, Liquid

- Device class: 1; regulation: 21 CFR 880.5090; FDA's rule: 510(k) required
- FDA decisions: 222
- 510(k) review time 2021–2025: median 88 days (middle half 88–88)
- Recalls: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2007: 2
- 2008: 3
- 2009: 3
- 2010: 1
- 2012: 1
- 2014: 2
- 2016: 2
- 2018: 1
- 2019: 1
- 2024: 1

## Most-cited predicates
- K984177: Modification to Skvekpatch (1998), cited by 10
- K965120: Allclenz Wound Cleanser (1997), cited by 8
- K945802: Dermagran Wound Cleanser with Zinc (1995), cited by 7
- K955453: Acticoat Silver Coated Dressing (1996), cited by 7
- K002338: Liquiderm Liquid Adhesive Bandage (2001), cited by 6
- K955103: 3M NO Sting Barrier Film (1996), cited by 5
- K013225: Instaclot for Otc Use, Traumasstat for Prescription Use (2001), cited by 5
- K022645: CURAD (2002), cited by 4
- K983833: Acticoat Composite Wound Dressing, Acticoat Composite Wound Dressing-Adhesive (1998), cited by 4
- K002550: RDH Bandage (2000), cited by 4

Source page: https://510kreport.com/product-code/KMF
Data by year (CSV): https://510kreport.com/product-code/KMF.csv