FDA 510(k)

BD Curve 腹水分流管

K号: K170405 · 2017-11-02

决定日期2017-11-02

产品代码KPM

咨询委员会GU 请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。

决定Unknown

器械摘要

BD Curve Ascites Shunt is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2017-11-02 under 510(k) number K170405. The device is classified under product code KPM. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常见问题

What is the BD Curve Ascites Shunt?

BD Curve Ascites Shunt is a medical device that received FDA 510(k) clearance on 2017-11-02. The listed applicant is Care Fusion. The 510(k) number is K170405.

When did BD Curve Ascites Shunt receive FDA 510(k) clearance?

BD Curve Ascites Shunt received FDA 510(k) clearance on 2017-11-02, under 510(k) number K170405.

Who is the listed applicant for BD Curve Ascites Shunt?

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

What is the FDA product code for BD Curve Ascites Shunt?

The FDA product code for BD Curve Ascites Shunt is KPM.

列明Care Fusion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。

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官方来源

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