TAP 刺针
K号: K223201 · 2023-04-19
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决定日期2023-04-19
产品代码FMK
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定Unknown
器械摘要
TAP Lancet is the device name listed in this FDA 510(k) record. The listed applicant is Yourbio Health, Inc.. It received FDA 510(k) clearance on 2023-04-19 under 510(k) number K223201. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Unknown.
常见问题
What is the TAP Lancet?
TAP Lancet is a medical device that received FDA 510(k) clearance on 2023-04-19. The listed applicant is Yourbio Health, Inc.. The 510(k) number is K223201.
When did TAP Lancet receive FDA 510(k) clearance?
TAP Lancet received FDA 510(k) clearance on 2023-04-19, under 510(k) number K223201.
Who is the listed applicant for TAP Lancet?
The FDA 510(k) record lists Yourbio Health, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TAP Lancet?
The FDA product code for TAP Lancet is FMK.
相关临床试验
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相关器械（代码：FMK）
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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