Axiom PX
K号: K161177 · 2017-06-15
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申请人Anthogyr Sas
决定日期2017-06-15
产品代码DZE
咨询委员会DE
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决定实质等同
器械摘要
Axiom PX is the device name listed in this FDA 510(k) record. The listed applicant is Anthogyr Sas. It received FDA 510(k) clearance on 2017-06-15 under 510(k) number K161177. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Axiom PX?
Axiom PX is a medical device that received FDA 510(k) clearance on 2017-06-15. The listed applicant is Anthogyr Sas. The 510(k) number is K161177.
When did Axiom PX receive FDA 510(k) clearance?
Axiom PX received FDA 510(k) clearance on 2017-06-15, under 510(k) number K161177.
Who is the listed applicant for Axiom PX?
The FDA 510(k) record lists Anthogyr Sas as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Axiom PX?
The FDA product code for Axiom PX is DZE.
相关临床试验
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相关器械（代码：DZE）
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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