FDA 510(k)

SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX

Número K: K210103 · 2021-07-16

RequerenteLifelong Meditech Private Limited

Data da decisão2021-07-16

Código do produtoFMF

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX 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 2021-07-16 under 510(k) number K210103. 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 SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?

SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX is a medical device that received FDA 510(k) clearance on 2021-07-16. The listed applicant is Lifelong Meditech Private Limited. The 510(k) number is K210103.

When did SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX receive FDA 510(k) clearance?

SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX received FDA 510(k) clearance on 2021-07-16, under 510(k) number K210103.

Who is the listed applicant for SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?

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 SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX?

The FDA product code for SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX is FMF.

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Fonte oficial

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