FDA 510(k)SurBlate消融系统
K号: K223272 · 2023-02-28
决定日期2023-02-28
产品代码NEY
咨询委员会SU
请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
SurBlate Ablation System is the device name listed in this FDA 510(k) record. The listed applicant is Mima-Pro Scientific, Inc.. It received FDA 510(k) clearance on 2023-02-28 under 510(k) number K223272. The device is classified under product code NEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SurBlate Ablation System?
SurBlate Ablation System is a medical device that received FDA 510(k) clearance on 2023-02-28. The listed applicant is Mima-Pro Scientific, Inc.. The 510(k) number is K223272.
When did SurBlate Ablation System receive FDA 510(k) clearance?
SurBlate Ablation System received FDA 510(k) clearance on 2023-02-28, under 510(k) number K223272.
Who is the listed applicant for SurBlate Ablation System?
The FDA 510(k) record lists Mima-Pro Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SurBlate Ablation System?
The FDA product code for SurBlate Ablation System is NEY.
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。
相关器械(代码:NEY)
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。
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