FDA 510(k)

vWF Ag

Número K: K220728 · 2023-06-02

RequerenteSiemens Healthcare Diagnostics Products GmbH

Data da decisão2023-06-02

Código do produtoGGP

Comité consultivoHE

DecisãoSubstantially Equivalent

Resumo do dispositivo

vWF Ag is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare Diagnostics Products GmbH. It received FDA 510(k) clearance on 2023-06-02 under 510(k) number K220728. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the vWF Ag?

vWF Ag is a medical device that received FDA 510(k) clearance on 2023-06-02. The listed applicant is Siemens Healthcare Diagnostics Products GmbH. The 510(k) number is K220728.

When did vWF Ag receive FDA 510(k) clearance?

vWF Ag received FDA 510(k) clearance on 2023-06-02, under 510(k) number K220728.

Who is the listed applicant for vWF Ag?

The FDA 510(k) record lists Siemens Healthcare Diagnostics Products GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for vWF Ag?

The FDA product code for vWF Ag is GGP.

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Fonte oficial

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