AccuFFRangio Plus
K号: K230303 · 2023-03-02
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器械摘要
AccuFFRangio Plus 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 2023-03-02 under 510(k) number K230303. The device is classified under product code QHA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AccuFFRangio Plus?
AccuFFRangio Plus is a medical device that received FDA 510(k) clearance on 2023-03-02. The listed applicant is ArteryFlow Technology Co., Ltd.. The 510(k) number is K230303.
When did AccuFFRangio Plus receive FDA 510(k) clearance?
AccuFFRangio Plus received FDA 510(k) clearance on 2023-03-02, under 510(k) number K230303.
Who is the listed applicant for AccuFFRangio Plus?
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 AccuFFRangio Plus?
The FDA product code for AccuFFRangio Plus is QHA.
相关临床试验
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列明ArteryFlow Technology Co., Ltd.为申报人的其他记录
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：QHA）
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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