LessGetChecked Impress
K号: K242680 · 2025-01-13
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决定日期2025-01-13
产品代码FMK
咨询委员会SU
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决定Unknown
器械摘要
LetsGetChecked Impress is the device name listed in this FDA 510(k) record. The listed applicant is Privapath Diagnostics Ltd (Dba Letsgetchecked). It received FDA 510(k) clearance on 2025-01-13 under 510(k) number K242680. 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 LetsGetChecked Impress?
LetsGetChecked Impress is a medical device that received FDA 510(k) clearance on 2025-01-13. The listed applicant is Privapath Diagnostics Ltd (Dba Letsgetchecked). The 510(k) number is K242680.
When did LetsGetChecked Impress receive FDA 510(k) clearance?
LetsGetChecked Impress received FDA 510(k) clearance on 2025-01-13, under 510(k) number K242680.
Who is the listed applicant for LetsGetChecked Impress?
The FDA 510(k) record lists Privapath Diagnostics Ltd (Dba Letsgetchecked) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LetsGetChecked Impress?
The FDA product code for LetsGetChecked Impress is FMK.
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：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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