FDA 510(k)

I.V. Administration Set, I.V. Extension Set

Número K: K223645 · 2023-05-18

Data da decisão2023-05-18

Código do produtoFPA

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

I.V. Administration Set, I.V. Extension Set is the device name listed in this FDA 510(k) record. The listed applicant is Bq Plus Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-05-18 under 510(k) number K223645. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the I.V. Administration Set, I.V. Extension Set?

I.V. Administration Set, I.V. Extension Set is a medical device that received FDA 510(k) clearance on 2023-05-18. The listed applicant is Bq Plus Medical Co., Ltd.. The 510(k) number is K223645.

When did I.V. Administration Set, I.V. Extension Set receive FDA 510(k) clearance?

I.V. Administration Set, I.V. Extension Set received FDA 510(k) clearance on 2023-05-18, under 510(k) number K223645.

Who is the listed applicant for I.V. Administration Set, I.V. Extension Set?

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

What is the FDA product code for I.V. Administration Set, I.V. Extension Set?

The FDA product code for I.V. Administration Set, I.V. Extension Set is FPA.

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Outros registros que listam Bq Plus Medical Co., Ltd. como candidato(a)

K242126I.V. Administration Set K210381I.V. Administration Set

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Fonte oficial

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