FDA 510(k)

AMT 缝线输送系统

K号: K193612 · 2020-03-12

决定日期2020-03-12

产品代码KGC

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决定实质等同

器械摘要

AMT Suture Delivery System 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 2020-03-12 under 510(k) number K193612. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the AMT Suture Delivery System?

AMT Suture Delivery System is a medical device that received FDA 510(k) clearance on 2020-03-12. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K193612.

When did AMT Suture Delivery System receive FDA 510(k) clearance?

AMT Suture Delivery System received FDA 510(k) clearance on 2020-03-12, under 510(k) number K193612.

Who is the listed applicant for AMT Suture Delivery System?

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 Suture Delivery System?

The FDA product code for AMT Suture Delivery System is KGC.

列明Applied Medical Technology, 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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官方来源

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