Apex定位器（AL-Pex），Apex定位器（AL-Pex+）
K号: K232717 · 2023-12-22
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器械摘要
Apex Locator (AL-Pex), Apex Locator (AL-Pex+) is the device name listed in this FDA 510(k) record. The listed applicant is Changzhou Haili Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-12-22 under 510(k) number K232717. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.
常见问题
What is the Apex Locator (AL-Pex), Apex Locator (AL-Pex+)?
Apex Locator (AL-Pex), Apex Locator (AL-Pex+) is a medical device that received FDA 510(k) clearance on 2023-12-22. The listed applicant is Changzhou Haili Medical Co., Ltd.. The 510(k) number is K232717.
When did Apex Locator (AL-Pex), Apex Locator (AL-Pex+) receive FDA 510(k) clearance?
Apex Locator (AL-Pex), Apex Locator (AL-Pex+) received FDA 510(k) clearance on 2023-12-22, under 510(k) number K232717.
Who is the listed applicant for Apex Locator (AL-Pex), Apex Locator (AL-Pex+)?
The FDA 510(k) record lists Changzhou Haili Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apex Locator (AL-Pex), Apex Locator (AL-Pex+)?
The FDA product code for Apex Locator (AL-Pex), Apex Locator (AL-Pex+) is LQY.
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。
相关器械（代码：LQY）
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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