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FDA 510(k)

数字口腔内X射线成像系统

K号: K212279 · 2021-10-07

决定日期2021-10-07
产品代码MUH
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决定实质等同

器械摘要

Digital Intraoral X-ray Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Iray Technology Taicang , Ltd.. It received FDA 510(k) clearance on 2021-10-07 under 510(k) number K212279. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Digital Intraoral X-ray Imaging System?

Digital Intraoral X-ray Imaging System is a medical device that received FDA 510(k) clearance on 2021-10-07. The listed applicant is Iray Technology Taicang , Ltd.. The 510(k) number is K212279.

When did Digital Intraoral X-ray Imaging System receive FDA 510(k) clearance?

Digital Intraoral X-ray Imaging System received FDA 510(k) clearance on 2021-10-07, under 510(k) number K212279.

Who is the listed applicant for Digital Intraoral X-ray Imaging System?

The FDA 510(k) record lists Iray Technology Taicang , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Digital Intraoral X-ray Imaging System?

The FDA product code for Digital Intraoral X-ray Imaging System is MUH.

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列明Iray Technology Taicang , Ltd.为申报人的其他记录

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相关器械(代码:MUH)

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

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