FDA 510(k)

Pristine Long-Term Hemodialysis Catheter

Número K: K203767 · 2021-04-02

Data da decisão2021-04-02

Código do produtoMSD

Comité consultivoGU

DecisãoUnknown

Resumo do dispositivo

Pristine Long-Term Hemodialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C B Bard, Inc.. It received FDA 510(k) clearance on 2021-04-02 under 510(k) number K203767. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Perguntas frequentes

What is the Pristine Long-Term Hemodialysis Catheter?

Pristine Long-Term Hemodialysis Catheter is a medical device that received FDA 510(k) clearance on 2021-04-02. The listed applicant is C B Bard, Inc.. The 510(k) number is K203767.

When did Pristine Long-Term Hemodialysis Catheter receive FDA 510(k) clearance?

Pristine Long-Term Hemodialysis Catheter received FDA 510(k) clearance on 2021-04-02, under 510(k) number K203767.

Who is the listed applicant for Pristine Long-Term Hemodialysis Catheter?

The FDA 510(k) record lists C B Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pristine Long-Term Hemodialysis Catheter?

The FDA product code for Pristine Long-Term Hemodialysis Catheter is MSD.

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Dispositivos Relacionados (Código: MSD)

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