DEKA LILY
K号: K233470 · 2023-12-19
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申请人El.En S.P.A.
决定日期2023-12-19
产品代码NGX
咨询委员会PM
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决定实质等同
器械摘要
DEKA LILY is the device name listed in this FDA 510(k) record. The listed applicant is El.En S.P.A.. It received FDA 510(k) clearance on 2023-12-19 under 510(k) number K233470. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DEKA LILY?
DEKA LILY is a medical device that received FDA 510(k) clearance on 2023-12-19. The listed applicant is El.En S.P.A.. The 510(k) number is K233470.
When did DEKA LILY receive FDA 510(k) clearance?
DEKA LILY received FDA 510(k) clearance on 2023-12-19, under 510(k) number K233470.
Who is the listed applicant for DEKA LILY?
The FDA 510(k) record lists El.En S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEKA LILY?
The FDA product code for DEKA LILY is NGX.
列明El.En S.P.A.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：NGX）
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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