Encision AEM Monopolar Laparoscopic Instruments and Accessories
K号: K191612 · 2020-03-20
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器械摘要
常见问题
What is the Encision AEM Monopolar Laparoscopic Instruments and Accessories?
Encision AEM Monopolar Laparoscopic Instruments and Accessories is a medical device that received FDA 510(k) clearance on 2020-03-20. The listed applicant is Encision Incorporated. The 510(k) number is K191612.
When did Encision AEM Monopolar Laparoscopic Instruments and Accessories receive FDA 510(k) clearance?
Encision AEM Monopolar Laparoscopic Instruments and Accessories received FDA 510(k) clearance on 2020-03-20, under 510(k) number K191612.
Who is the listed applicant for Encision AEM Monopolar Laparoscopic Instruments and Accessories?
The FDA 510(k) record lists Encision Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Encision AEM Monopolar Laparoscopic Instruments and Accessories?
The FDA product code for Encision AEM Monopolar Laparoscopic Instruments and Accessories is GEI.
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:GEI)
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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