GIA 钉合器带三钉技术
K号: K202701 · 2020-12-07
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器械摘要
GIA Stapler with Tri-Staple Technology is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2020-12-07 under 510(k) number K202701. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the GIA Stapler with Tri-Staple Technology?
GIA Stapler with Tri-Staple Technology is a medical device that received FDA 510(k) clearance on 2020-12-07. The listed applicant is Covidien. The 510(k) number is K202701.
When did GIA Stapler with Tri-Staple Technology receive FDA 510(k) clearance?
GIA Stapler with Tri-Staple Technology received FDA 510(k) clearance on 2020-12-07, under 510(k) number K202701.
Who is the listed applicant for GIA Stapler with Tri-Staple Technology?
The FDA 510(k) record lists Covidien as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GIA Stapler with Tri-Staple Technology?
The FDA product code for GIA Stapler with Tri-Staple Technology is GDW.
相关临床试验
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。
列明Covidien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。
相关器械（代码：GDW）
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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