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FDA 510(k)

Salem Sump 双腔胃管带 ENFit 连接

K号: K190923 · 2019-11-07

决定日期2019-11-07
产品代码PIF
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。
决定实质等同

器械摘要

Salem Sump Dual Lumen Stomach Tube with ENFit Connection is the device name listed in this FDA 510(k) record. The listed applicant is Cardinalhealth. It received FDA 510(k) clearance on 2019-11-07 under 510(k) number K190923. The device is classified under product code PIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Salem Sump Dual Lumen Stomach Tube with ENFit Connection?

Salem Sump Dual Lumen Stomach Tube with ENFit Connection is a medical device that received FDA 510(k) clearance on 2019-11-07. The listed applicant is Cardinalhealth. The 510(k) number is K190923.

When did Salem Sump Dual Lumen Stomach Tube with ENFit Connection receive FDA 510(k) clearance?

Salem Sump Dual Lumen Stomach Tube with ENFit Connection received FDA 510(k) clearance on 2019-11-07, under 510(k) number K190923.

Who is the listed applicant for Salem Sump Dual Lumen Stomach Tube with ENFit Connection?

FDA 510(k)记录显示Cardinalhealth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 Salem Sump Dual Lumen Stomach Tube with ENFit Connection?

The FDA product code for Salem Sump Dual Lumen Stomach Tube with ENFit Connection is PIF.

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Cardinalhealth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:PIF)

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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