FDA 510(k)

Perifix and Contiplex Catheter

Número K: K153297 · 2016-08-12

Data da decisão2016-08-12

Código do produtoBSO

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Perifix and Contiplex Catheter is the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2016-08-12 under 510(k) number K153297. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Perifix and Contiplex Catheter?

Perifix and Contiplex Catheter is a medical device that received FDA 510(k) clearance on 2016-08-12. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K153297.

When did Perifix and Contiplex Catheter receive FDA 510(k) clearance?

Perifix and Contiplex Catheter received FDA 510(k) clearance on 2016-08-12, under 510(k) number K153297.

Who is the listed applicant for Perifix and Contiplex Catheter?

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

What is the FDA product code for Perifix and Contiplex Catheter?

The FDA product code for Perifix and Contiplex Catheter is BSO.

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Fonte oficial

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