FDA 510(k)

Retractable Safety Insulin Syringe

Número K: K193022 · 2020-07-20

Data da decisão2020-07-20

Código do produtoMEG

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Retractable Safety Insulin 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 2020-07-20 under 510(k) number K193022. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Retractable Safety Insulin Syringe?

Retractable Safety Insulin Syringe is a medical device that received FDA 510(k) clearance on 2020-07-20. The listed applicant is Jiangsu Caina Medical Co.,Ltd. The 510(k) number is K193022.

When did Retractable Safety Insulin Syringe receive FDA 510(k) clearance?

Retractable Safety Insulin Syringe received FDA 510(k) clearance on 2020-07-20, under 510(k) number K193022.

Who is the listed applicant for Retractable Safety Insulin 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 Retractable Safety Insulin Syringe?

The FDA product code for Retractable Safety Insulin Syringe is MEG.

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Fonte oficial

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