PHAROS
K号: K250170 · 2025-08-15
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器械摘要
PHAROS is the device name listed in this FDA 510(k) record. The listed applicant is Brightonix Imaging. It received FDA 510(k) clearance on 2025-08-15 under 510(k) number K250170. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PHAROS?
PHAROS is a medical device that received FDA 510(k) clearance on 2025-08-15. The listed applicant is Brightonix Imaging. The 510(k) number is K250170.
When did PHAROS receive FDA 510(k) clearance?
PHAROS received FDA 510(k) clearance on 2025-08-15, under 510(k) number K250170.
Who is the listed applicant for PHAROS?
The FDA 510(k) record lists Brightonix Imaging as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHAROS?
The FDA product code for PHAROS is KPS.
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。
相关器械（代码：KPS）
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。
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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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