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FDA 510(k)

Medwell Technology Ltd Syringes, various sizes

Número K: K212764 · 2022-11-04

RequerenteMedwell Technology, Ltd.
Data da decisão2022-11-04
Código do produtoFMF
Comité consultivoHO
DecisãoSubstantially Equivalent

Resumo do dispositivo

Medwell Technology Ltd Syringes, various sizes is the device name listed in this FDA 510(k) record. The listed applicant is Medwell Technology, Ltd.. It received FDA 510(k) clearance on 2022-11-04 under 510(k) number K212764. 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 Medwell Technology Ltd Syringes, various sizes?

Medwell Technology Ltd Syringes, various sizes is a medical device that received FDA 510(k) clearance on 2022-11-04. The listed applicant is Medwell Technology, Ltd.. The 510(k) number is K212764.

When did Medwell Technology Ltd Syringes, various sizes receive FDA 510(k) clearance?

Medwell Technology Ltd Syringes, various sizes received FDA 510(k) clearance on 2022-11-04, under 510(k) number K212764.

Who is the listed applicant for Medwell Technology Ltd Syringes, various sizes?

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

What is the FDA product code for Medwell Technology Ltd Syringes, various sizes?

The FDA product code for Medwell Technology Ltd Syringes, various sizes is FMF.

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