neuromate Gen III
K号: K180206 · 2018-04-24
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决定日期2018-04-24
产品代码HAW
咨询委员会NE
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器械摘要
neuromate Gen III is the device name listed in this FDA 510(k) record. The listed applicant is Renishaw Mayfield Sarl. It received FDA 510(k) clearance on 2018-04-24 under 510(k) number K180206. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the neuromate Gen III?
neuromate Gen III is a medical device that received FDA 510(k) clearance on 2018-04-24. The listed applicant is Renishaw Mayfield Sarl. The 510(k) number is K180206.
When did neuromate Gen III receive FDA 510(k) clearance?
neuromate Gen III received FDA 510(k) clearance on 2018-04-24, under 510(k) number K180206.
Who is the listed applicant for neuromate Gen III?
The FDA 510(k) record lists Renishaw Mayfield Sarl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for neuromate Gen III?
The FDA product code for neuromate Gen III is HAW.
相关临床试验
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列明Renishaw Mayfield Sarl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：HAW）
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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