外科现实查看器
K号: K252091 · 2026-01-29
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器械摘要
Surgical Reality Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Medicalvr B.V.. It received FDA 510(k) clearance on 2026-01-29 under 510(k) number K252091. 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 Surgical Reality Viewer?
Surgical Reality Viewer is a medical device that received FDA 510(k) clearance on 2026-01-29. The listed applicant is Medicalvr B.V.. The 510(k) number is K252091.
When did Surgical Reality Viewer receive FDA 510(k) clearance?
Surgical Reality Viewer received FDA 510(k) clearance on 2026-01-29, under 510(k) number K252091.
Who is the listed applicant for Surgical Reality Viewer?
The FDA 510(k) record lists Medicalvr B.V. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Surgical Reality Viewer?
The FDA product code for Surgical Reality Viewer 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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