MicroTrend System
K号: K212425 · 2024-11-07
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决定日期2024-11-07
产品代码CCK
咨询委员会AN
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器械摘要
MicroTrend System is the device name listed in this FDA 510(k) record. The listed applicant is Exostat Medical, Inc.. It received FDA 510(k) clearance on 2024-11-07 under 510(k) number K212425. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MicroTrend System?
MicroTrend System is a medical device that received FDA 510(k) clearance on 2024-11-07. The listed applicant is Exostat Medical, Inc.. The 510(k) number is K212425.
When did MicroTrend System receive FDA 510(k) clearance?
MicroTrend System received FDA 510(k) clearance on 2024-11-07, under 510(k) number K212425.
Who is the listed applicant for MicroTrend System?
The FDA 510(k) record lists Exostat Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MicroTrend System?
The FDA product code for MicroTrend System is CCK.
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：CCK）
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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