CryoProbe™ CryoProbe XP+

• FDA 510(k) K024009 decided 20 Mar 2003 Active
• FDA GUDID UDI-DI 15407008481527 listed 10 Mar 2025 Listed

1. 20 Mar 2003 Cleared FDA 510(k) K024009
2. 10 Mar 2025 Listed FDA GUDID 15407008481527

Trade name

CryoProbe™

Generic name

General cryosurgical system, cryogen gas, mechanical

Model / Ref / Catalog

CryoProbe XP+, S-HO-CEPRPLUS-00

Primary DI / UDI-DI

15407008481527

510(k) Number

K024009 ↗

FDA product code

GEH

GMDN term

General cryosurgical system, cryogen gas, mechanical

Device class

Class II

Regulation number

878.4350

GUDID distribution status

In Commercial Distribution

Category: General cryosurgical system, cryogen gas, mechanical

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See all devices from H & O Equipments SA →