FDA 510(k)

Unipro（K-UNIPRO-US）

K号: K232441 · 2024-08-30

决定日期2024-08-30

产品代码GZJ

咨询委员会NE 请注意，您提供的文本“NE”不足以进行翻译，因为它不是一个完整的句子或描述。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。

决定实质等同

器械摘要

Unipro (K-UNIPRO-US) is the device name listed in this FDA 510(k) record. The listed applicant is Tenscare, Ltd.. It received FDA 510(k) clearance on 2024-08-30 under 510(k) number K232441. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Unipro (K-UNIPRO-US)?

Unipro (K-UNIPRO-US) is a medical device that received FDA 510(k) clearance on 2024-08-30. The listed applicant is Tenscare, Ltd.. The 510(k) number is K232441.

When did Unipro (K-UNIPRO-US) receive FDA 510(k) clearance?

Unipro (K-UNIPRO-US) received FDA 510(k) clearance on 2024-08-30, under 510(k) number K232441.

Who is the listed applicant for Unipro (K-UNIPRO-US)?

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

What is the FDA product code for Unipro (K-UNIPRO-US)?

The FDA product code for Unipro (K-UNIPRO-US) is GZJ.

列明Tenscare, 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。

K230926年轻女性卵巢保留适应性放射治疗试验 K230983优康（K-UNICARE-USA）K231053优康（K-UNICARE-USA）K200694Perfect EMS K191312Perfect PFE

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。