FDA 510(k)

Apollo TMS 疗法系统；Apollo light TMS 疗法系统

K号: K260560 · 2026-05-22

决定日期2026-05-22

产品代码OBP

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决定实质等同

器械摘要

Apollo TMS Therapy System;Apollo light TMS Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Mag & More GmbH. It received FDA 510(k) clearance on 2026-05-22 under 510(k) number K260560. 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 Apollo TMS Therapy System;Apollo light TMS Therapy System?

Apollo TMS Therapy System;Apollo light TMS Therapy System is a medical device that received FDA 510(k) clearance on 2026-05-22. The listed applicant is Mag & More GmbH. The 510(k) number is K260560.

When did Apollo TMS Therapy System;Apollo light TMS Therapy System receive FDA 510(k) clearance?

Apollo TMS Therapy System;Apollo light TMS Therapy System received FDA 510(k) clearance on 2026-05-22, under 510(k) number K260560.

Who is the listed applicant for Apollo TMS Therapy System;Apollo light TMS Therapy System?

The FDA 510(k) record lists Mag & More GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Apollo TMS Therapy System;Apollo light TMS Therapy System?

The FDA product code for Apollo TMS Therapy System;Apollo light TMS Therapy System is OBP.

列明Mag & More GmbH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。

K243700Apollo TMS 疗法系统 K243539Apollo TMS 疗法系统 K232639Apollo TMS 疗法系统 K180313Apollo TMS 疗法系统

官方来源

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