EQ-PEX
K号: K210789 · 2021-10-20
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器械摘要
EQ-PEX is the device name listed in this FDA 510(k) record. The listed applicant is Meta Systems Co., Ltd.. It received FDA 510(k) clearance on 2021-10-20 under 510(k) number K210789. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.
常见问题
What is the EQ-PEX?
EQ-PEX is a medical device that received FDA 510(k) clearance on 2021-10-20. The listed applicant is Meta Systems Co., Ltd.. The 510(k) number is K210789.
When did EQ-PEX receive FDA 510(k) clearance?
EQ-PEX received FDA 510(k) clearance on 2021-10-20, under 510(k) number K210789.
Who is the listed applicant for EQ-PEX?
The FDA 510(k) record lists Meta Systems Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EQ-PEX?
The FDA product code for EQ-PEX is LQY.
列明Meta Systems Co., Ltd.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：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.K231990Apex定位器Cefla S.C.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.
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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