AiORTA - Plan v2.0
K号: K254207 · 2026-03-30
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器械摘要
AiORTA - Plan v2.0 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 2026-03-30 under 510(k) number K254207. 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 v2.0?
AiORTA - Plan v2.0 is a medical device that received FDA 510(k) clearance on 2026-03-30. The listed applicant is ViTAA Medical Solutions, Inc.. The 510(k) number is K254207.
When did AiORTA - Plan v2.0 receive FDA 510(k) clearance?
AiORTA - Plan v2.0 received FDA 510(k) clearance on 2026-03-30, under 510(k) number K254207.
Who is the listed applicant for AiORTA - Plan v2.0?
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 v2.0?
The FDA product code for AiORTA - Plan v2.0 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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