# K052259: DR. Scholl's Dual Action Freeze Away Wart Remover, Model 40406

- Pathway: 510(k) (Traditional)
- Applicant: Schering-Plough Healthcare Products, Inc.
- Decided: Dec 14, 2005 after 117 days
- Product code: GEH (Unit, Cryosurgical, Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4350
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K911420 (1991). 7 ancestors in all.
1 later device descends from it; 1 cites 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)
- K031697: DR. Scholl's Freeze Away Wart Remover, Model 40226, Schering-Plough Healthcare Products, Inc. (2003) Summary page 1.
- K980739: Histofreezer/ 17% Salicylic Acid-Verruca Plantaris, OraSure Technologies, Inc. (1998) Summary page 1.

## Most influential descendants
- K161294: Compound W Wart Removal System Dual Power (2016), 0 descendants of its own

## Indications for use
For the removal of common and plantar warts.

Source page: https://510kreport.com/device/K052259
Methodology: https://510kreport.com/methodology