AiORTA - 计划
K号: K250337 · 2025-10-30
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器械摘要
AiORTA - Plan is the device name listed in this FDA 510(k) record. The listed applicant is ViTAA Medical Solutions, Inc.. It received FDA 510(k) clearance on 2025-10-30 under 510(k) number K250337. 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 AiORTA - Plan?
AiORTA - Plan is a medical device that received FDA 510(k) clearance on 2025-10-30. The listed applicant is ViTAA Medical Solutions, Inc.. The 510(k) number is K250337.
When did AiORTA - Plan receive FDA 510(k) clearance?
AiORTA - Plan received FDA 510(k) clearance on 2025-10-30, under 510(k) number K250337.
Who is the listed applicant for AiORTA - Plan?
The FDA 510(k) record lists ViTAA Medical Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AiORTA - Plan?
The FDA product code for AiORTA - Plan is QIH.
相关临床试验
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列明ViTAA Medical Solutions, Inc.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：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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