STATSTIX
K号: K200764 · 2020-10-15
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器械摘要
STATSTIX is the device name listed in this FDA 510(k) record. The listed applicant is Centrix Incorporated. It received FDA 510(k) clearance on 2020-10-15 under 510(k) number K200764. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.
常见问题
What is the STATSTIX?
STATSTIX is a medical device that received FDA 510(k) clearance on 2020-10-15. The listed applicant is Centrix Incorporated. The 510(k) number is K200764.
When did STATSTIX receive FDA 510(k) clearance?
STATSTIX received FDA 510(k) clearance on 2020-10-15, under 510(k) number K200764.
Who is the listed applicant for STATSTIX?
The FDA 510(k) record lists Centrix Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STATSTIX?
The FDA product code for STATSTIX is MVL.
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：MVL）
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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