XTRA4
K号: K251320 · 2025-09-11
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器械摘要
XTRA4 is the device name listed in this FDA 510(k) record. The listed applicant is Al.Chi.Mi.A. S.R.L. It received FDA 510(k) clearance on 2025-09-11 under 510(k) number K251320. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.
常见问题
What is the XTRA4?
XTRA4 is a medical device that received FDA 510(k) clearance on 2025-09-11. The listed applicant is Al.Chi.Mi.A. S.R.L. The 510(k) number is K251320.
When did XTRA4 receive FDA 510(k) clearance?
XTRA4 received FDA 510(k) clearance on 2025-09-11, under 510(k) number K251320.
Who is the listed applicant for XTRA4?
The FDA 510(k) record lists Al.Chi.Mi.A. S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XTRA4?
The FDA product code for XTRA4 is LYX.
列明Al.Chi.Mi.A. S.R.L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：LYX）
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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