Inzii Ripstop 可重部署回收系统
K号: K232880 · 2023-11-01
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器械摘要
常见问题
What is the Inzii Ripstop Redeployable Retrieval System?
Inzii Ripstop Redeployable Retrieval System is a medical device that received FDA 510(k) clearance on 2023-11-01. The listed applicant is Applied Medical Resources Corporation. The 510(k) number is K232880.
When did Inzii Ripstop Redeployable Retrieval System receive FDA 510(k) clearance?
Inzii Ripstop Redeployable Retrieval System received FDA 510(k) clearance on 2023-11-01, under 510(k) number K232880.
Who is the listed applicant for Inzii Ripstop Redeployable Retrieval System?
The FDA 510(k) record lists Applied Medical Resources Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Inzii Ripstop Redeployable Retrieval System?
The FDA product code for Inzii Ripstop Redeployable Retrieval System is GCJ.
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Applied Medical Resources Corporation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：GCJ）
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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