# K243454: Verruca-Freeze H

- Pathway: 510(k) (Special)
- Applicant: Cryosurgery, Inc.
- Decided: Dec 3, 2024 after 26 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 K990877 (1999). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233347: Verruca-Freeze® H, Cryosurgery, Inc. (2023) Summary page 5.

## Most influential descendants
- K252903: Verruca-Freeze H Plus (2025), 0 descendants of its own

## Indications for use
The Verruca-Freeze@ H cryosurgical system is indicated for use in the treatment of the following skin lesions: *Actinic Keratosis * Genital Warts * Lentigo * Molluscum Contagiosum * Seborrheic Keratosis * Skin Tags *Verruca Plantaris *Verruca Vulgaris *Verruca Plana

Source page: https://510kreport.com/device/K243454
Methodology: https://510kreport.com/methodology