FDA 510(k)

Echotip Ultra 内镜支气管高清超声针，Echotip Procore 内镜支气管高清超声活检针

K号: K160229 · 2016-03-21

决定日期2016-03-21

产品代码FCG

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决定实质等同

器械摘要

Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ireland, Ltd.. It received FDA 510(k) clearance on 2016-03-21 under 510(k) number K160229. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle?

Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle is a medical device that received FDA 510(k) clearance on 2016-03-21. The listed applicant is Cook Ireland, Ltd.. The 510(k) number is K160229.

When did Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle receive FDA 510(k) clearance?

Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle received FDA 510(k) clearance on 2016-03-21, under 510(k) number K160229.

Who is the listed applicant for Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle?

FDA 510(k)记录中列出Cook Ireland, Ltd.为申请人。这本身并不能确立该设备的制造商。

What is the FDA product code for Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle?

The FDA product code for Echotip Ultra Endobronchial High Definition Ultrasound Needle, Echotip Procore Endobronchial High Definition Ultrasound Biopsy Needle is FCG.

列明Cook Ireland, Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K261274EchoTip Ultra® 内镜超声活检针，适用于富士胶片内窥镜；EchoTip ProCore® 内镜超声活检针，适用于富士胶片内窥镜 K241209EchoTip AcuCore™ EUS 细胞活检针 (ECHO-BX-19)K233079Zimmon® 胰腺支架/支架套装（SPSOF，SPSOS，ZEPDF，ZEPDS，ZPSOF，ZPSOS）；Geenen® 胰腺支架/支架套装（GEPD，GPDS，GPSO，GPSOS）；Johlin® 胰腺楔形支架和导引器套装（JPWS）；推送导管和导引导管（GC，PC）；Geenen® Sof-Flex® 胰腺支架（GPSO-SF，GPSOS-SF）K230909EchoTip® AcuCore™ 超声活检针 (ECHO-BX-3-22)K213946Compass BDS 胆管支架 K210476EchoTip Ultra 内镜超声针，EchoTip ProCore HD 超声活检针，EchoTip Ultra 内镜支气管高清晰度超声针，EchoTip ProCore 内镜支气管高清晰度活检针

查看所有 16 个设备 →

官方来源

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数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。