FDA 510(k)

Kit/Conjunto de Cateter de Bloqueio Periférico Contínuo FlexBlock ARROW

Número K: K153652 · 2016-06-21

Data da decisão2016-06-21

Código do produtoCAZ

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex, Inc.. It received FDA 510(k) clearance on 2016-06-21 under 510(k) number K153652. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set?

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set is a medical device that received FDA 510(k) clearance on 2016-06-21. The listed applicant is Teleflex, Inc.. The 510(k) number is K153652.

When did ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set receive FDA 510(k) clearance?

ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set received FDA 510(k) clearance on 2016-06-21, under 510(k) number K153652.

Who is the listed applicant for ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set?

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

What is the FDA product code for ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set?

The FDA product code for ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set is CAZ.

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