Phoenix Clinical ICON
K号: K170527 · 2017-09-15
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决定日期2017-09-15
产品代码HKI
咨询委员会OP
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决定实质等同
器械摘要
Phoenix Clinical ICON is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Technology Group, Inc. Dba Phoenix Clinical. It received FDA 510(k) clearance on 2017-09-15 under 510(k) number K170527. The device is classified under product code HKI. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Phoenix Clinical ICON?
Phoenix Clinical ICON is a medical device that received FDA 510(k) clearance on 2017-09-15. The listed applicant is Phoenix Technology Group, Inc. Dba Phoenix Clinical. The 510(k) number is K170527.
When did Phoenix Clinical ICON receive FDA 510(k) clearance?
Phoenix Clinical ICON received FDA 510(k) clearance on 2017-09-15, under 510(k) number K170527.
Who is the listed applicant for Phoenix Clinical ICON?
The FDA 510(k) record lists Phoenix Technology Group, Inc. Dba Phoenix Clinical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Phoenix Clinical ICON?
The FDA product code for Phoenix Clinical ICON is HKI.
相关临床试验
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相关器械（代码：HKI）
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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