Medipoint 血液刀片
K号: K223480 · 2023-01-13
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决定日期2023-01-13
产品代码QRK
咨询委员会SU
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器械摘要
Medipoint Blood Lancets is the device name listed in this FDA 510(k) record. The listed applicant is Medipoint Holdings, LLC. It received FDA 510(k) clearance on 2023-01-13 under 510(k) number K223480. The device is classified under product code QRK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Medipoint Blood Lancets?
Medipoint Blood Lancets is a medical device that received FDA 510(k) clearance on 2023-01-13. The listed applicant is Medipoint Holdings, LLC. The 510(k) number is K223480.
When did Medipoint Blood Lancets receive FDA 510(k) clearance?
Medipoint Blood Lancets received FDA 510(k) clearance on 2023-01-13, under 510(k) number K223480.
Who is the listed applicant for Medipoint Blood Lancets?
The FDA 510(k) record lists Medipoint Holdings, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medipoint Blood Lancets?
The FDA product code for Medipoint Blood Lancets is QRK.
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：QRK）
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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