FDA 510(k)

Pump Alignment Syringe

Número K: K220184 · 2022-07-21

Data da decisão2022-07-21

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Pump Alignment Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Caina Medical Co.,Ltd. It received FDA 510(k) clearance on 2022-07-21 under 510(k) number K220184. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Pump Alignment Syringe?

Pump Alignment Syringe is a medical device that received FDA 510(k) clearance on 2022-07-21. The listed applicant is Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K220184.

When did Pump Alignment Syringe receive FDA 510(k) clearance?

Pump Alignment Syringe received FDA 510(k) clearance on 2022-07-21, under 510(k) number K220184.

Who is the listed applicant for Pump Alignment Syringe?

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

What is the FDA product code for Pump Alignment Syringe?

The FDA product code for Pump Alignment Syringe is FMF.

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Fonte oficial

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