S698 Symbioz 流量
K号: K153367 · 2016-06-17
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决定日期2016-06-17
产品代码HIF
咨询委员会OB
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决定实质等同
器械摘要
S698 Symbioz flow is the device name listed in this FDA 510(k) record. The listed applicant is Sopro - Acteon Group. It received FDA 510(k) clearance on 2016-06-17 under 510(k) number K153367. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the S698 Symbioz flow?
S698 Symbioz flow is a medical device that received FDA 510(k) clearance on 2016-06-17. The listed applicant is Sopro - Acteon Group. The 510(k) number is K153367.
When did S698 Symbioz flow receive FDA 510(k) clearance?
S698 Symbioz flow received FDA 510(k) clearance on 2016-06-17, under 510(k) number K153367.
Who is the listed applicant for S698 Symbioz flow?
The FDA 510(k) record lists Sopro - Acteon Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for S698 Symbioz flow?
The FDA product code for S698 Symbioz flow is HIF.
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：HIF）
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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