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FDA 510(k)

Blood Collection Needles

Número K: K200932 · 2021-12-14

RequerenteVacutest Kima Srl
Data da decisão2021-12-14
Código do produtoFMI
Comité consultivoHO
DecisãoSubstantially Equivalent

Resumo do dispositivo

Blood Collection Needles is the device name listed in this FDA 510(k) record. The listed applicant is Vacutest Kima Srl. It received FDA 510(k) clearance on 2021-12-14 under 510(k) number K200932. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Blood Collection Needles?

Blood Collection Needles is a medical device that received FDA 510(k) clearance on 2021-12-14. The listed applicant is Vacutest Kima Srl. The 510(k) number is K200932.

When did Blood Collection Needles receive FDA 510(k) clearance?

Blood Collection Needles received FDA 510(k) clearance on 2021-12-14, under 510(k) number K200932.

Who is the listed applicant for Blood Collection Needles?

The FDA 510(k) record lists Vacutest Kima Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Blood Collection Needles?

The FDA product code for Blood Collection Needles is FMI.

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Dispositivos Relacionados (Código: FMI)

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