Dose+ (1.0)
K号: K250064 · 2025-09-04
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器械摘要
Dose+ (1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Mvision AI OY. It received FDA 510(k) clearance on 2025-09-04 under 510(k) number K250064. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Dose+ (1.0)?
Dose+ (1.0) is a medical device that received FDA 510(k) clearance on 2025-09-04. The listed applicant is Mvision AI OY. The 510(k) number is K250064.
When did Dose+ (1.0) receive FDA 510(k) clearance?
Dose+ (1.0) received FDA 510(k) clearance on 2025-09-04, under 510(k) number K250064.
Who is the listed applicant for Dose+ (1.0)?
The FDA 510(k) record lists Mvision AI OY as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dose+ (1.0)?
The FDA product code for Dose+ (1.0) is MUJ.
列明Mvision AI OY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：MUJ）
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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