X-View 3D全景/X-View 2D全景
K号: K222666 · 2023-07-10
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器械摘要
X-View 3D Pan/X-View 2D Pan is the device name listed in this FDA 510(k) record. The listed applicant is Trident S.R.L. It received FDA 510(k) clearance on 2023-07-10 under 510(k) number K222666. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the X-View 3D Pan/X-View 2D Pan?
X-View 3D Pan/X-View 2D Pan is a medical device that received FDA 510(k) clearance on 2023-07-10. The listed applicant is Trident S.R.L. The 510(k) number is K222666.
When did X-View 3D Pan/X-View 2D Pan receive FDA 510(k) clearance?
X-View 3D Pan/X-View 2D Pan received FDA 510(k) clearance on 2023-07-10, under 510(k) number K222666.
Who is the listed applicant for X-View 3D Pan/X-View 2D Pan?
The FDA 510(k) record lists Trident S.R.L as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for X-View 3D Pan/X-View 2D Pan?
The FDA product code for X-View 3D Pan/X-View 2D Pan is OAS.
列明Trident S.R.L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：OAS）
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
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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