RemedyLogic AI 腰椎 MRI 读取器
K号: K241108 · 2024-10-30
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器械摘要
RemedyLogic AI MRI Lumbar Spine Reader is the device name listed in this FDA 510(k) record. The listed applicant is Remedy Logic, Inc.. It received FDA 510(k) clearance on 2024-10-30 under 510(k) number K241108. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the RemedyLogic AI MRI Lumbar Spine Reader?
RemedyLogic AI MRI Lumbar Spine Reader is a medical device that received FDA 510(k) clearance on 2024-10-30. The listed applicant is Remedy Logic, Inc.. The 510(k) number is K241108.
When did RemedyLogic AI MRI Lumbar Spine Reader receive FDA 510(k) clearance?
RemedyLogic AI MRI Lumbar Spine Reader received FDA 510(k) clearance on 2024-10-30, under 510(k) number K241108.
Who is the listed applicant for RemedyLogic AI MRI Lumbar Spine Reader?
The FDA 510(k) record lists Remedy Logic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RemedyLogic AI MRI Lumbar Spine Reader?
The FDA product code for RemedyLogic AI MRI Lumbar Spine Reader is QIH.
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：QIH）
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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