SC Medica FFX
K号: K232468 · 2024-05-09
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器械摘要
SC Medica FFX is the device name listed in this FDA 510(k) record. The listed applicant is Sc Medica. It received FDA 510(k) clearance on 2024-05-09 under 510(k) number K232468. The device is classified under product code MRW. FDA Decision: Substantially Equivalent.
常见问题
What is the SC Medica FFX?
SC Medica FFX is a medical device that received FDA 510(k) clearance on 2024-05-09. The listed applicant is Sc Medica. The 510(k) number is K232468.
When did SC Medica FFX receive FDA 510(k) clearance?
SC Medica FFX received FDA 510(k) clearance on 2024-05-09, under 510(k) number K232468.
Who is the listed applicant for SC Medica FFX?
The FDA 510(k) record lists Sc Medica as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SC Medica FFX?
The FDA product code for SC Medica FFX is MRW.
相关临床试验
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列明Sc Medica为申报人的其他记录
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相关器械（代码：MRW）
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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