胃肠道边界标识器（GIBI HD）
K号: K221898 · 2022-07-28
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器械摘要
常见问题
What is the Gastrointestinal Boundary Identifier (GIBI HD)?
Gastrointestinal Boundary Identifier (GIBI HD) is a medical device that received FDA 510(k) clearance on 2022-07-28. The listed applicant is Reshape Lifesciences. The 510(k) number is K221898.
When did Gastrointestinal Boundary Identifier (GIBI HD) receive FDA 510(k) clearance?
Gastrointestinal Boundary Identifier (GIBI HD) received FDA 510(k) clearance on 2022-07-28, under 510(k) number K221898.
Who is the listed applicant for Gastrointestinal Boundary Identifier (GIBI HD)?
The FDA 510(k) record lists Reshape Lifesciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Gastrointestinal Boundary Identifier (GIBI HD)?
The FDA product code for Gastrointestinal Boundary Identifier (GIBI HD) is KNT.
相关临床试验
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列明Reshape Lifesciences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：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
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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