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FDA 510(k)

ISP安全胡贝尔注射针输液套装

K号: K170881 · 2017-12-14

决定日期2017-12-14
产品代码PTI
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

ISP Safety Huber Needle Infusion Set is the device name listed in this FDA 510(k) record. The listed applicant is Infusion Safety Products, Inc.. It received FDA 510(k) clearance on 2017-12-14 under 510(k) number K170881. The device is classified under product code PTI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ISP Safety Huber Needle Infusion Set?

ISP Safety Huber Needle Infusion Set is a medical device that received FDA 510(k) clearance on 2017-12-14. The listed applicant is Infusion Safety Products, Inc.. The 510(k) number is K170881.

When did ISP Safety Huber Needle Infusion Set receive FDA 510(k) clearance?

ISP Safety Huber Needle Infusion Set received FDA 510(k) clearance on 2017-12-14, under 510(k) number K170881.

Who is the listed applicant for ISP Safety Huber Needle Infusion Set?

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

What is the FDA product code for ISP Safety Huber Needle Infusion Set?

The FDA product code for ISP Safety Huber Needle Infusion Set is PTI.

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:PTI)

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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