FDA 510(k)

Recon Support Catheter

Número K: K203275 · 2021-03-01

Data da decisão2021-03-01

Código do produtoDQY

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Recon Support 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 2021-03-01 under 510(k) number K203275. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Recon Support Catheter?

Recon Support Catheter is a medical device that received FDA 510(k) clearance on 2021-03-01. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K203275.

When did Recon Support Catheter receive FDA 510(k) clearance?

Recon Support Catheter received FDA 510(k) clearance on 2021-03-01, under 510(k) number K203275.

Who is the listed applicant for Recon Support 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 Recon Support Catheter?

The FDA product code for Recon Support Catheter is DQY.

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Fonte oficial

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