FDA 510(k)

RIA Safeguard

Número K: K222416 · 2023-05-01

Data da decisão2023-05-01

Código do produtoFRF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

RIA Safeguard is the device name listed in this FDA 510(k) record. The listed applicant is Ria Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-05-01 under 510(k) number K222416. The device is classified under product code FRF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the RIA Safeguard?

RIA Safeguard is a medical device that received FDA 510(k) clearance on 2023-05-01. The listed applicant is Ria Tech Co., Ltd.. The 510(k) number is K222416.

When did RIA Safeguard receive FDA 510(k) clearance?

RIA Safeguard received FDA 510(k) clearance on 2023-05-01, under 510(k) number K222416.

Who is the listed applicant for RIA Safeguard?

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

What is the FDA product code for RIA Safeguard?

The FDA product code for RIA Safeguard is FRF.

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