FDA 510(k)

Rapid2 疗法系统

K号: K162935 · 2017-03-10

决定日期2017-03-10

产品代码OBP

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决定实质等同

器械摘要

Rapid2 Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Magstim Company, Ltd.. It received FDA 510(k) clearance on 2017-03-10 under 510(k) number K162935. The device is classified under product code OBP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Rapid2 Therapy System?

Rapid2 Therapy System is a medical device that received FDA 510(k) clearance on 2017-03-10. The listed applicant is Magstim Company, Ltd.. The 510(k) number is K162935.

When did Rapid2 Therapy System receive FDA 510(k) clearance?

Rapid2 Therapy System received FDA 510(k) clearance on 2017-03-10, under 510(k) number K162935.

Who is the listed applicant for Rapid2 Therapy System?

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

What is the FDA product code for Rapid2 Therapy System?

The FDA product code for Rapid2 Therapy System is OBP.

列明Magstim Company, 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。

K223154Magstim Horizon 3.0 TMS治疗系统，Horizon 3.0系统，Horizon 3.0，H3.0，Horizon 3.0 with StimGuide+K222171Magstim Horizon 3.0 TMS治疗系统，Horizon 3.0系统，Horizon 3.0，H3.0，Horizon 3.0 with StimGuide+K211389Magstim Horizon 3.0 TMS治疗系统，Horizon 3.0系统，Horizon 3.0，Horizon 3.0 with Navigation K203684Neurosign V4术中神经监护仪 K183376HORIZON TMS 疗法系统带导航 K182853HORIZON TMS 疗法系统

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官方来源

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