FDA 510(k)

Cope儿科胃肠道缝合锚定器套装，造口缝合锚定器套装

K号: K182832 · 2019-06-26

决定日期2019-06-26

产品代码KGC

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Unknown

器械摘要

Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2019-06-26 under 510(k) number K182832. The device is classified under product code KGC. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

常见问题

What is the Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set?

Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set is a medical device that received FDA 510(k) clearance on 2019-06-26. The listed applicant is Cook Incorporated. The 510(k) number is K182832.

When did Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set receive FDA 510(k) clearance?

Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set received FDA 510(k) clearance on 2019-06-26, under 510(k) number K182832.

Who is the listed applicant for Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set?

The FDA 510(k) record lists Cook Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set?

The FDA product code for Cope Pediatric Gastrointestinal Suture Anchor Set, Enterostomy Suture Anchor Set is KGC.

列明Cook Incorporated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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