CAPENERGY - C100, C200, C300, C400, C50
K号: K191202 · 2020-02-11
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器械摘要
常见问题
What is the CAPENERGY - C100, C200, C300, C400, C50?
CAPENERGY - C100, C200, C300, C400, C50 is a medical device that received FDA 510(k) clearance on 2020-02-11. The listed applicant is Capenergy Medical S.L.. The 510(k) number is K191202.
When did CAPENERGY - C100, C200, C300, C400, C50 receive FDA 510(k) clearance?
CAPENERGY - C100, C200, C300, C400, C50 received FDA 510(k) clearance on 2020-02-11, under 510(k) number K191202.
Who is the listed applicant for CAPENERGY - C100, C200, C300, C400, C50?
The FDA 510(k) record lists Capenergy Medical S.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAPENERGY - C100, C200, C300, C400, C50?
The FDA product code for CAPENERGY - C100, C200, C300, C400, C50 is PBX.
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Capenergy Medical S.L.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:PBX)
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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