FDA 510(k)

Pulse Oximeter ( PO2, PO2A, PO2B)

Número K: K242876 · 2025-02-28

RequerenteShenzhen Viatom Technology Co., Ltd.

Data da decisão2025-02-28

Código do produtoDQA

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Pulse Oximeter ( PO2, PO2A, PO2B) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Viatom Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-02-28 under 510(k) number K242876. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Pulse Oximeter ( PO2, PO2A, PO2B)?

Pulse Oximeter ( PO2, PO2A, PO2B) is a medical device that received FDA 510(k) clearance on 2025-02-28. The listed applicant is Shenzhen Viatom Technology Co., Ltd.. The 510(k) number is K242876.

When did Pulse Oximeter ( PO2, PO2A, PO2B) receive FDA 510(k) clearance?

Pulse Oximeter ( PO2, PO2A, PO2B) received FDA 510(k) clearance on 2025-02-28, under 510(k) number K242876.

Who is the listed applicant for Pulse Oximeter ( PO2, PO2A, PO2B)?

The FDA 510(k) record lists Shenzhen Viatom Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pulse Oximeter ( PO2, PO2A, PO2B)?

The FDA product code for Pulse Oximeter ( PO2, PO2A, PO2B) is DQA.

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Outros registros que listam Shenzhen Viatom Technology Co., Ltd. como candidato(a)

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Dispositivos Relacionados (Código: DQA)

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Fonte oficial

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