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FDA 510(k)

NAR Sharps Shuttle; NAR Sharps Shuttle 六件套

K号: K152340 · 2016-05-31

决定日期2016-05-31
产品代码MMK
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six is the device name listed in this FDA 510(k) record. The listed applicant is North American Rescue, LLC. It received FDA 510(k) clearance on 2016-05-31 under 510(k) number K152340. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six?

NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six is a medical device that received FDA 510(k) clearance on 2016-05-31. The listed applicant is North American Rescue, LLC. The 510(k) number is K152340.

When did NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six receive FDA 510(k) clearance?

NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six received FDA 510(k) clearance on 2016-05-31, under 510(k) number K152340.

Who is the listed applicant for NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six?

The FDA 510(k) record lists North American Rescue, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six?

The FDA product code for NAR Sharps Shuttle; NAR Sharps Shuttle Pack of six is MMK.

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:MMK)

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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