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FDA 510(k)

AMT G-Tube 气囊胃造口喂养装置

K号: K222846 · 2023-12-18

决定日期2023-12-18
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。
决定实质等同

器械摘要

AMT G-Tube Balloon Gastrostomy Feeding Device is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technology, Inc.. It received FDA 510(k) clearance on 2023-12-18 under 510(k) number K222846. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AMT G-Tube Balloon Gastrostomy Feeding Device?

AMT G-Tube Balloon Gastrostomy Feeding Device is a medical device that received FDA 510(k) clearance on 2023-12-18. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K222846.

When did AMT G-Tube Balloon Gastrostomy Feeding Device receive FDA 510(k) clearance?

AMT G-Tube Balloon Gastrostomy Feeding Device received FDA 510(k) clearance on 2023-12-18, under 510(k) number K222846.

Who is the listed applicant for AMT G-Tube Balloon Gastrostomy Feeding Device?

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

What is the FDA product code for AMT G-Tube Balloon Gastrostomy Feeding Device?

The FDA product code for AMT G-Tube Balloon Gastrostomy Feeding Device is KNT.

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列明Applied Medical Technology, Inc.为申报人的其他记录

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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。

官方来源

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