AccuCTP
K号: K220663 · 2022-11-22
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器械摘要
AccuCTP is the device name listed in this FDA 510(k) record. The listed applicant is ArteryFlow Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-11-22 under 510(k) number K220663. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AccuCTP?
AccuCTP is a medical device that received FDA 510(k) clearance on 2022-11-22. The listed applicant is ArteryFlow Technology Co., Ltd.. The 510(k) number is K220663.
When did AccuCTP receive FDA 510(k) clearance?
AccuCTP received FDA 510(k) clearance on 2022-11-22, under 510(k) number K220663.
Who is the listed applicant for AccuCTP?
The FDA 510(k) record lists ArteryFlow Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AccuCTP?
The FDA product code for AccuCTP is LLZ.
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列明ArteryFlow Technology Co., Ltd.为申报人的其他记录
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相关器械（代码：LLZ）
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
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