星射频电极，VIVA射频电极
K号: K172012 · 2018-03-14
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器械摘要
star RF Electrode, VIVA RF Electrode is the device name listed in this FDA 510(k) record. The listed applicant is Starmed Co., Ltd.. It received FDA 510(k) clearance on 2018-03-14 under 510(k) number K172012. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the star RF Electrode, VIVA RF Electrode?
star RF Electrode, VIVA RF Electrode is a medical device that received FDA 510(k) clearance on 2018-03-14. The listed applicant is Starmed Co., Ltd.. The 510(k) number is K172012.
When did star RF Electrode, VIVA RF Electrode receive FDA 510(k) clearance?
star RF Electrode, VIVA RF Electrode received FDA 510(k) clearance on 2018-03-14, under 510(k) number K172012.
Who is the listed applicant for star RF Electrode, VIVA RF Electrode?
The FDA 510(k) record lists Starmed Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for star RF Electrode, VIVA RF Electrode?
The FDA product code for star RF Electrode, VIVA RF Electrode 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。
列明Starmed Co., Ltd.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：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。
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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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