FDA 510(k)

Xoran工作站，型號10050

K 號：K210257 · 2021-05-20

決定日期2021-05-20

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

Xoran Workstation, Model 10050 is the device name listed in this FDA 510(k) record. The listed applicant is Xoran Technologies, LLC. It received FDA 510(k) clearance on 2021-05-20 under 510(k) number K210257. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Xoran Workstation, Model 10050?

Xoran Workstation, Model 10050 is a medical device that received FDA 510(k) clearance on 2021-05-20. The listed applicant is Xoran Technologies, LLC. The 510(k) number is K210257.

When did Xoran Workstation, Model 10050 receive FDA 510(k) clearance?

Xoran Workstation, Model 10050 received FDA 510(k) clearance on 2021-05-20, under 510(k) number K210257.

Who is the listed applicant for Xoran Workstation, Model 10050?

The FDA 510(k) record lists Xoran Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Xoran Workstation, Model 10050?

The FDA product code for Xoran Workstation, Model 10050 is LLZ.

其他以 Xoran Technologies, LLC 為申請人之記錄

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相關器械（代碼：LLZ）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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