LUNA 3D
K号: K232031 · 2024-03-29
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器械摘要
LUNA 3D is the device name listed in this FDA 510(k) record. The listed applicant is Lap GmbH Laser Applikationen. It received FDA 510(k) clearance on 2024-03-29 under 510(k) number K232031. 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 LUNA 3D?
LUNA 3D is a medical device that received FDA 510(k) clearance on 2024-03-29. The listed applicant is Lap GmbH Laser Applikationen. The 510(k) number is K232031.
When did LUNA 3D receive FDA 510(k) clearance?
LUNA 3D received FDA 510(k) clearance on 2024-03-29, under 510(k) number K232031.
Who is the listed applicant for LUNA 3D?
The FDA 510(k) record lists Lap GmbH Laser Applikationen as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LUNA 3D?
The FDA product code for LUNA 3D is IYE.
列明Lap GmbH Laser Applikationen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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