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FDA 510(k)

PleurX 腹膜导管系统

K号: K201155 · 2020-10-21

申请人Care Fusion
决定日期2020-10-21
产品代码PNG
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

PleurX Peritoneal Catheter System is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2020-10-21 under 510(k) number K201155. The device is classified under product code PNG. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常见问题

What is the PleurX Peritoneal Catheter System?

PleurX Peritoneal Catheter System is a medical device that received FDA 510(k) clearance on 2020-10-21. The listed applicant is Care Fusion. The 510(k) number is K201155.

When did PleurX Peritoneal Catheter System receive FDA 510(k) clearance?

PleurX Peritoneal Catheter System received FDA 510(k) clearance on 2020-10-21, under 510(k) number K201155.

Who is the listed applicant for PleurX Peritoneal Catheter System?

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 PleurX Peritoneal Catheter System?

The FDA product code for PleurX Peritoneal Catheter System is PNG.

相关临床试验

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。

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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相关器械(代码:PNG)

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。

官方来源

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