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FDA 510(k)

CORGRIP NG/NI管固定系统

K号: K162110 · 2016-09-15

决定日期2016-09-15
产品代码KNT
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

CORGRIP NG/NI Tube Retention System is the device name listed in this FDA 510(k) record. The listed applicant is Corpak Medsystems, Inc. A Division of Haylard Health. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K162110. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常见问题

What is the CORGRIP NG/NI Tube Retention System?

CORGRIP NG/NI Tube Retention System is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Corpak Medsystems, Inc. A Division of Haylard Health. The 510(k) number is K162110.

When did CORGRIP NG/NI Tube Retention System receive FDA 510(k) clearance?

CORGRIP NG/NI Tube Retention System received FDA 510(k) clearance on 2016-09-15, under 510(k) number K162110.

Who is the listed applicant for CORGRIP NG/NI Tube Retention System?

The FDA 510(k) record lists Corpak Medsystems, Inc. A Division of Haylard Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORGRIP NG/NI Tube Retention System?

The FDA product code for CORGRIP NG/NI Tube Retention System is KNT.

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。

相关器械(代码:KNT)

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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