FDA 510(k)

Removendor de Verrugas Cryo Avançado

Número K: K242288 · 2025-01-21

RequerenteMedical Brands Laboratories B.V.

Data da decisão2025-01-21

Código do produtoGEH

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Advanced Cryo Wart Remover is the device name listed in this FDA 510(k) record. The listed applicant is Medical Brands Laboratories B.V.. It received FDA 510(k) clearance on 2025-01-21 under 510(k) number K242288. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Advanced Cryo Wart Remover?

Advanced Cryo Wart Remover is a medical device that received FDA 510(k) clearance on 2025-01-21. The listed applicant is Medical Brands Laboratories B.V.. The 510(k) number is K242288.

When did Advanced Cryo Wart Remover receive FDA 510(k) clearance?

Advanced Cryo Wart Remover received FDA 510(k) clearance on 2025-01-21, under 510(k) number K242288.

Who is the listed applicant for Advanced Cryo Wart Remover?

The FDA 510(k) record lists Medical Brands Laboratories B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Advanced Cryo Wart Remover?

The FDA product code for Advanced Cryo Wart Remover is GEH.

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Outros registros que listam Medical Brands Laboratories B.V. como candidato(a)

K252198Removendorrugas a Crisoterapia Avançado (Removendorrugas Avançado)

Dispositivos Relacionados (Código: GEH)

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Fonte oficial

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