FDA 510(k)

Auto Disable Syringe

Número K: K210464 · 2021-08-24

RequerenteAnhui Tiankang Medical Technology Co., Ltd.

Data da decisão2021-08-24

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Auto Disable Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-08-24 under 510(k) number K210464. 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 Auto Disable Syringe?

Auto Disable Syringe is a medical device that received FDA 510(k) clearance on 2021-08-24. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. The 510(k) number is K210464.

When did Auto Disable Syringe receive FDA 510(k) clearance?

Auto Disable Syringe received FDA 510(k) clearance on 2021-08-24, under 510(k) number K210464.

Who is the listed applicant for Auto Disable Syringe?

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

What is the FDA product code for Auto Disable Syringe?

The FDA product code for Auto Disable Syringe is FMF.

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Outros registros que listam Anhui Tiankang Medical Technology Co., Ltd. como candidato(a)

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Fonte oficial

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