Apex定位器
K号: K231990 · 2024-02-13
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器械摘要
Apex Locator is the device name listed in this FDA 510(k) record. The listed applicant is Cefla S.C.. It received FDA 510(k) clearance on 2024-02-13 under 510(k) number K231990. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.
常见问题
What is the Apex Locator?
Apex Locator is a medical device that received FDA 510(k) clearance on 2024-02-13. The listed applicant is Cefla S.C.. The 510(k) number is K231990.
When did Apex Locator receive FDA 510(k) clearance?
Apex Locator received FDA 510(k) clearance on 2024-02-13, under 510(k) number K231990.
Who is the listed applicant for Apex Locator?
The FDA 510(k) record lists Cefla S.C. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Apex Locator?
The FDA product code for Apex Locator 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。
列明Cefla S.C.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。
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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。
K252224Apex定位器（FindPex）Changzhou Sifary Medical Technology Co., Ltd.K242383Apex定位器Shenzhen Rogin Medical Co., Ltd.K242765电子尖端定位器（Alpha Apex I）SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.K232717Apex定位器（AL-Pex），Apex定位器（AL-Pex+）Changzhou Haili Medical Co., Ltd.K212178根尖定位器Foshan Coxo Medical Instrument Co., Ltd.K210789EQ-PEXMeta Systems Co., Ltd.
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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