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FDA 510(k)

AMSure 肠内喂养泵

K号: K220230 · 2022-11-10

决定日期2022-11-10
产品代码LZH
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

AMSure Enteral Feeding Pump is the device name listed in this FDA 510(k) record. The listed applicant is Amsino International, Inc.. It received FDA 510(k) clearance on 2022-11-10 under 510(k) number K220230. The device is classified under product code LZH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AMSure Enteral Feeding Pump?

AMSure Enteral Feeding Pump is a medical device that received FDA 510(k) clearance on 2022-11-10. The listed applicant is Amsino International, Inc.. The 510(k) number is K220230.

When did AMSure Enteral Feeding Pump receive FDA 510(k) clearance?

AMSure Enteral Feeding Pump received FDA 510(k) clearance on 2022-11-10, under 510(k) number K220230.

Who is the listed applicant for AMSure Enteral Feeding Pump?

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

What is the FDA product code for AMSure Enteral Feeding Pump?

The FDA product code for AMSure Enteral Feeding Pump is LZH.

相关临床试验

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列明Amsino International, 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。

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相关器械(代码:LZH)

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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