FDA 510(k)

AccuCath Intravascular Catheter

Número K: K162894 · 2016-11-15

Data da decisão2016-11-15

Código do produtoFOZ

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

AccuCath Intravascular 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 2016-11-15 under 510(k) number K162894. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the AccuCath Intravascular Catheter?

AccuCath Intravascular Catheter is a medical device that received FDA 510(k) clearance on 2016-11-15. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162894.

When did AccuCath Intravascular Catheter receive FDA 510(k) clearance?

AccuCath Intravascular Catheter received FDA 510(k) clearance on 2016-11-15, under 510(k) number K162894.

Who is the listed applicant for AccuCath Intravascular 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 AccuCath Intravascular Catheter?

The FDA product code for AccuCath Intravascular Catheter is FOZ.

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