FDA 510(k)Certus 140 2.45GHz 消融系统
K号: K160936 · 2016-05-04
决定日期2016-05-04
产品代码NEY
咨询委员会SU
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决定实质等同
器械摘要
Certus 140 2.45GHz Ablation System is the device name listed in this FDA 510(k) record. The listed applicant is Neuwave Medical, Inc.. It received FDA 510(k) clearance on 2016-05-04 under 510(k) number K160936. 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 Certus 140 2.45GHz Ablation System?
Certus 140 2.45GHz Ablation System is a medical device that received FDA 510(k) clearance on 2016-05-04. The listed applicant is Neuwave Medical, Inc.. The 510(k) number is K160936.
When did Certus 140 2.45GHz Ablation System receive FDA 510(k) clearance?
Certus 140 2.45GHz Ablation System received FDA 510(k) clearance on 2016-05-04, under 510(k) number K160936.
Who is the listed applicant for Certus 140 2.45GHz Ablation System?
The FDA 510(k) record lists Neuwave Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Certus 140 2.45GHz Ablation System?
The FDA product code for Certus 140 2.45GHz Ablation System is NEY.
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列明Neuwave Medical, Inc.为申报人的其他记录
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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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