FDA 510(k)

GlidePath 7.5F Long-Term Dialysis Catheter

Número K: K202150 · 2020-11-18

Data da decisão2020-11-18

Código do produtoMSD

Comité consultivoGU

DecisãoUnknown

Resumo do dispositivo

GlidePath 7.5F Long-Term Dialysis Catheter is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2020-11-18 under 510(k) number K202150. The device is classified under product code MSD. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Perguntas frequentes

What is the GlidePath 7.5F Long-Term Dialysis Catheter?

GlidePath 7.5F Long-Term Dialysis Catheter is a medical device that received FDA 510(k) clearance on 2020-11-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K202150.

When did GlidePath 7.5F Long-Term Dialysis Catheter receive FDA 510(k) clearance?

GlidePath 7.5F Long-Term Dialysis Catheter received FDA 510(k) clearance on 2020-11-18, under 510(k) number K202150.

Who is the listed applicant for GlidePath 7.5F Long-Term Dialysis Catheter?

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

What is the FDA product code for GlidePath 7.5F Long-Term Dialysis Catheter?

The FDA product code for GlidePath 7.5F Long-Term Dialysis Catheter is MSD.

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Fonte oficial

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