MagVita TMS治疗系统
K号: K171481 · 2017-06-16
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器械摘要
常见问题
What is the MagVita TMS Therapy System?
MagVita TMS Therapy System is a medical device that received FDA 510(k) clearance on 2017-06-16. The listed applicant is Tonica Elektronik A/S. The 510(k) number is K171481.
When did MagVita TMS Therapy System receive FDA 510(k) clearance?
MagVita TMS Therapy System received FDA 510(k) clearance on 2017-06-16, under 510(k) number K171481.
Who is the listed applicant for MagVita TMS Therapy System?
The FDA 510(k) record lists Tonica Elektronik A/S as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MagVita TMS Therapy System?
The FDA product code for MagVita TMS Therapy System is OBP.
相关临床试验
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列明Tonica Elektronik A/S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:OBP)
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。
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