FDA 510(k)

ARROW FlexBlock 连续外周神经阻滞导管套装

K 號：K153652 · 2016-06-21

決定日期2016-06-21

產品代碼CAZ

諮詢委員會AN

決定相當於

器材摘要

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.

常見問題

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.

相關器械（代碼：CAZ）

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：CAZ）

官方來源