FDA 510(k)

Bifurcated Needle

Número K: K222385 · 2022-12-06

RequerenteAnhui Tiankang Medical Technology Co., Ltd.

Data da decisão2022-12-06

Código do produtoSCL

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Bifurcated Needle 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 2022-12-06 under 510(k) number K222385. The device is classified under product code SCL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Bifurcated Needle?

Bifurcated Needle is a medical device that received FDA 510(k) clearance on 2022-12-06. The listed applicant is Anhui Tiankang Medical Technology Co., Ltd.. The 510(k) number is K222385.

When did Bifurcated Needle receive FDA 510(k) clearance?

Bifurcated Needle received FDA 510(k) clearance on 2022-12-06, under 510(k) number K222385.

Who is the listed applicant for Bifurcated Needle?

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 Bifurcated Needle?

The FDA product code for Bifurcated Needle is SCL.

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Fonte oficial

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