Lunit INSIGHT MMG (v1.1.10)
K号: K260320 · 2026-04-23
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器械摘要
Lunit INSIGHT MMG (v1.1.10) is the device name listed in this FDA 510(k) record. The listed applicant is Lunit, Inc.. It received FDA 510(k) clearance on 2026-04-23 under 510(k) number K260320. The device is classified under product code QDQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Lunit INSIGHT MMG (v1.1.10)?
Lunit INSIGHT MMG (v1.1.10) is a medical device that received FDA 510(k) clearance on 2026-04-23. The listed applicant is Lunit, Inc.. The 510(k) number is K260320.
When did Lunit INSIGHT MMG (v1.1.10) receive FDA 510(k) clearance?
Lunit INSIGHT MMG (v1.1.10) received FDA 510(k) clearance on 2026-04-23, under 510(k) number K260320.
Who is the listed applicant for Lunit INSIGHT MMG (v1.1.10)?
The FDA 510(k) record lists Lunit, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lunit INSIGHT MMG (v1.1.10)?
The FDA product code for Lunit INSIGHT MMG (v1.1.10) is QDQ.
相关临床试验
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列明Lunit, 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：QDQ）
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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