LIA Console (542-7)
K号: K251730 · 2025-12-19
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器械摘要
LIA Console (542-7) is the device name listed in this FDA 510(k) record. The listed applicant is Leadoptik, Inc.. It received FDA 510(k) clearance on 2025-12-19 under 510(k) number K251730. The device is classified under product code NQQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LIA Console (542-7)?
LIA Console (542-7) is a medical device that received FDA 510(k) clearance on 2025-12-19. The listed applicant is Leadoptik, Inc.. The 510(k) number is K251730.
When did LIA Console (542-7) receive FDA 510(k) clearance?
LIA Console (542-7) received FDA 510(k) clearance on 2025-12-19, under 510(k) number K251730.
Who is the listed applicant for LIA Console (542-7)?
The FDA 510(k) record lists Leadoptik, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIA Console (542-7)?
The FDA product code for LIA Console (542-7) is NQQ.
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。
列明Leadoptik, Inc.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：NQQ）
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。
K253459OPTIS 移动 Next 成像系统 (1014932)；OPTIS 集成 Next 成像系统 (1014933)；Ultreon 3.0 软件升级套件 (ULTR300001)ABBOTT MEDICALK253101HyperVue™成像系统 - 集成Spectrawave, Inc.K252851deepLive（OSP12 + DMS）Damae MedicalK251198HyperVue™软件Spectrawave, Inc.K250684OPUSWAVE 双传感器成像系统Terumo Cardiovascular Systems Thi PlantK242924OPXION 光学皮肤观察器 (OPXSV1-01F)Opxion Technology, Inc.
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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