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FDA 510(k)

AMSure 预充水球膨胀注射器

K号: K181814 · 2018-09-04

决定日期2018-09-04
产品代码EZL
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

AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water 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 2018-09-04 under 510(k) number K181814. The device is classified under product code EZL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water?

AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water is a medical device that received FDA 510(k) clearance on 2018-09-04. The listed applicant is Amsino International, Inc.. The 510(k) number is K181814.

When did AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water receive FDA 510(k) clearance?

AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water received FDA 510(k) clearance on 2018-09-04, under 510(k) number K181814.

Who is the listed applicant for AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water?

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 Pre-filled Syringe for Balloon Inflation with Sterile Water?

The FDA product code for AMSure Pre-filled Syringe for Balloon Inflation with Sterile Water is EZL.

相关临床试验

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列明Amsino International, Inc.为申报人的其他记录

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相关器械(代码:EZL)

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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