Fibroid Mapping Reviewer Application (FMRA)
K号: K222683 · 2023-07-17
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器械摘要
Fibroid Mapping Reviewer Application (FMRA) is the device name listed in this FDA 510(k) record. The listed applicant is Nesa Medtech Private Limited. It received FDA 510(k) clearance on 2023-07-17 under 510(k) number K222683. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Fibroid Mapping Reviewer Application (FMRA)?
Fibroid Mapping Reviewer Application (FMRA) is a medical device that received FDA 510(k) clearance on 2023-07-17. The listed applicant is Nesa Medtech Private Limited. The 510(k) number is K222683.
When did Fibroid Mapping Reviewer Application (FMRA) receive FDA 510(k) clearance?
Fibroid Mapping Reviewer Application (FMRA) received FDA 510(k) clearance on 2023-07-17, under 510(k) number K222683.
Who is the listed applicant for Fibroid Mapping Reviewer Application (FMRA)?
The FDA 510(k) record lists Nesa Medtech Private Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fibroid Mapping Reviewer Application (FMRA)?
The FDA product code for Fibroid Mapping Reviewer Application (FMRA) is LLZ.
相关临床试验
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相关器械（代码：LLZ）
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
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