StrokeSENS LVO
K号: K212261 · 2021-10-14
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器械摘要
StrokeSENS LVO is the device name listed in this FDA 510(k) record. The listed applicant is Circle Neurovascular Imaging, Inc.. It received FDA 510(k) clearance on 2021-10-14 under 510(k) number K212261. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the StrokeSENS LVO?
StrokeSENS LVO is a medical device that received FDA 510(k) clearance on 2021-10-14. The listed applicant is Circle Neurovascular Imaging, Inc.. The 510(k) number is K212261.
When did StrokeSENS LVO receive FDA 510(k) clearance?
StrokeSENS LVO received FDA 510(k) clearance on 2021-10-14, under 510(k) number K212261.
Who is the listed applicant for StrokeSENS LVO?
The FDA 510(k) record lists Circle Neurovascular Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for StrokeSENS LVO?
The FDA product code for StrokeSENS LVO is QAS.
相关临床试验
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相关器械（代码：QAS）
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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