MOSAIC 3D（手术激光）
K号: K233550 · 2024-01-02
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决定日期2024-01-02
产品代码ONG
咨询委员会SU
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器械摘要
MOSAIC 3D (Surgical Laser) is the device name listed in this FDA 510(k) record. The listed applicant is Lutronic Aesthetic. It received FDA 510(k) clearance on 2024-01-02 under 510(k) number K233550. The device is classified under product code ONG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MOSAIC 3D (Surgical Laser)?
MOSAIC 3D (Surgical Laser) is a medical device that received FDA 510(k) clearance on 2024-01-02. The listed applicant is Lutronic Aesthetic. The 510(k) number is K233550.
When did MOSAIC 3D (Surgical Laser) receive FDA 510(k) clearance?
MOSAIC 3D (Surgical Laser) received FDA 510(k) clearance on 2024-01-02, under 510(k) number K233550.
Who is the listed applicant for MOSAIC 3D (Surgical Laser)?
The FDA 510(k) record lists Lutronic Aesthetic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOSAIC 3D (Surgical Laser)?
The FDA product code for MOSAIC 3D (Surgical Laser) is ONG.
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相关器械（代码：ONG）
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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