LIAC S
K号: K182374 · 2019-05-22
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器械摘要
LIAC S is the device name listed in this FDA 510(k) record. The listed applicant is Sit Sordina Iort Technologies Spa. It received FDA 510(k) clearance on 2019-05-22 under 510(k) number K182374. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LIAC S?
LIAC S is a medical device that received FDA 510(k) clearance on 2019-05-22. The listed applicant is Sit Sordina Iort Technologies Spa. The 510(k) number is K182374.
When did LIAC S receive FDA 510(k) clearance?
LIAC S received FDA 510(k) clearance on 2019-05-22, under 510(k) number K182374.
Who is the listed applicant for LIAC S?
The FDA 510(k) record lists Sit Sordina Iort Technologies Spa as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIAC S?
The FDA product code for LIAC S is IYE.
列明Sit Sordina Iort Technologies Spa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：IYE）
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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