FDA 510(k)

Hypodermic Syringes & Needle

Número K: K222925 · 2023-07-18

RequerenteLifelong Meditech Private Limited

Data da decisão2023-07-18

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Hypodermic Syringes & Needle is the device name listed in this FDA 510(k) record. The listed applicant is Lifelong Meditech Private Limited. It received FDA 510(k) clearance on 2023-07-18 under 510(k) number K222925. 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 Hypodermic Syringes & Needle?

Hypodermic Syringes & Needle is a medical device that received FDA 510(k) clearance on 2023-07-18. The listed applicant is Lifelong Meditech Private Limited. The 510(k) number is K222925.

When did Hypodermic Syringes & Needle receive FDA 510(k) clearance?

Hypodermic Syringes & Needle received FDA 510(k) clearance on 2023-07-18, under 510(k) number K222925.

Who is the listed applicant for Hypodermic Syringes & Needle?

The FDA 510(k) record lists Lifelong Meditech Private Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Hypodermic Syringes & Needle?

The FDA product code for Hypodermic Syringes & Needle is FMF.

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Outros registros que listam Lifelong Meditech Private Limited como candidato(a)

K210103SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX

Dispositivos Relacionados (Código: FMF)

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Fonte oficial

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