免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

疼痛治疗设备(SM9075,SM9910,SM9067,SM9587W)

K号: K233092 · 2024-02-12

决定日期2024-02-12
产品代码NUH
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

Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W) is the device name listed in this FDA 510(k) record. The listed applicant is Chongqing Rob Linka Science and Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-02-12 under 510(k) number K233092. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W)?

Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W) is a medical device that received FDA 510(k) clearance on 2024-02-12. The listed applicant is Chongqing Rob Linka Science and Technology Co., Ltd.. The 510(k) number is K233092.

When did Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W) receive FDA 510(k) clearance?

Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W) received FDA 510(k) clearance on 2024-02-12, under 510(k) number K233092.

Who is the listed applicant for Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W)?

The FDA 510(k) record lists Chongqing Rob Linka Science and Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W)?

The FDA product code for Pain Therapy Device (SM9075, SM9910, SM9067, SM9587W) is NUH.

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Chongqing Rob Linka Science and Technology 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:NUH)

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。

↑