FDA 510(k)

LAA 排除系统

K号: K232295 · 2023-08-30

决定日期2023-08-30

产品代码PZX

咨询委员会SU 请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。

决定实质等同

器械摘要

LAA Exclusion System is the device name listed in this FDA 510(k) record. The listed applicant is Syntheon, LLC. It received FDA 510(k) clearance on 2023-08-30 under 510(k) number K232295. The device is classified under product code PZX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LAA Exclusion System?

LAA Exclusion System is a medical device that received FDA 510(k) clearance on 2023-08-30. The listed applicant is Syntheon, LLC. The 510(k) number is K232295.

When did LAA Exclusion System receive FDA 510(k) clearance?

LAA Exclusion System received FDA 510(k) clearance on 2023-08-30, under 510(k) number K232295.

Who is the listed applicant for LAA Exclusion System?

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

What is the FDA product code for LAA Exclusion System?

The FDA product code for LAA Exclusion System is PZX.

相关器械（代码：PZX）

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。

器械摘要

常见问题

相关临床试验

相关器械（代码：PZX）

官方来源