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FDA 510(k)

COMPACTCATH 润滑间歇导尿管和 OneCath 间歇导尿管

K号: K180738 · 2018-06-14

决定日期2018-06-14
产品代码EZD
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

COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Compactcath, Inc.. It received FDA 510(k) clearance on 2018-06-14 under 510(k) number K180738. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter?

COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter is a medical device that received FDA 510(k) clearance on 2018-06-14. The listed applicant is Compactcath, Inc.. The 510(k) number is K180738.

When did COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter receive FDA 510(k) clearance?

COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter received FDA 510(k) clearance on 2018-06-14, under 510(k) number K180738.

Who is the listed applicant for COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter?

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

What is the FDA product code for COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter?

The FDA product code for COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary Catheter is EZD.

相关临床试验

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列明Compactcath, Inc.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。

相关器械(代码:EZD)

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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