# K022645: CURAD

- Pathway: 510(k) (Traditional)
- Applicant: Beiersdorf AG
- Decided: Nov 5, 2002 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
Longest line of descent: 1 generation back to K002338 (2001). 1 ancestor in all.
16 later devices descend from it; 4 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002338: Liquiderm Liquid Adhesive Bandage, Closure Medical Corp. (2001) Summary page 1.

## Most influential descendants
- K032948: Elastic Skin Liquid Bandage (2004), 8 descendants of its own
- K042610: DR. Theiss Alergol Pollen Blocker Cream (2005), 7 descendants of its own
- K053625: Nasalguard (2006), 6 descendants of its own
- K132520: Nasal Ease Allergy Blocker (2013), 3 descendants of its own
- K083913: Chesson Labs Liquid Bandage (2009), 3 descendants of its own

## Indications for use
CURAD® Spray Bandage is indicated for providing a covering over minor cuts and scrapes that are clean and dry.

Source page: https://510kreport.com/device/K022645
Methodology: https://510kreport.com/methodology