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510(k) Data Aggregation

    K Number
    K252903
    Manufacturer
    Date Cleared
    2025-10-10

    (29 days)

    Product Code
    Regulation Number
    878.4350
    Reference & Predicate Devices
    Predicate For
    N/A
    Why did this record match?
    Reference Devices :

    K233347

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Verruca-Freeze H Plus cryosurgical system is intended for use by trained medical professionals to treat the following benign skin lesions:

    • Actinic Keratosis
    • Genital Warts
    • Lentigo
    • Molluscum Contagiosum
    • Seborrheic Keratosis
    • Skin Tags
    • Verruca Plantaris
    • Verruca Vulgaris
    • Verruca Plana
    Device Description

    The main component of the Verruca-Freeze® H Plus cryosurgical system is the pressurized aerosol canister containing cryogen spray. The canister is used with foam swabs, which are non-sterile, single-use applicators that are disposed of after each use. The foam swabs allow the cryogen to be localized to a target lesion.

    The procedure begins by saturating a foam swab with cryogen and then placing it directly onto the lesion for 15–40 seconds. Upon removal of the swab from the skin, the frozen tissue appears white and begins thawing. The typical thaw time is 20–40 seconds. This treatment methodology is simple and has been an accepted practice used by physicians for decades. It utilizes a cryogen formulation to freeze lesions and destroy the underlying tissue through evaporative cooling. On the cellular level, both extracellular and intracellular ice formation occur. This submission includes a modification to the cryogen formulation. No other changes were made to the device design, intended use, or operating principle.

    AI/ML Overview

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