FDA 510(k)

TRON

K 號：K221230 · 2022-07-28

決定日期2022-07-28

產品代碼OWB

諮詢委員會RA

決定相當於

器材摘要

TRON 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 2022-07-28 under 510(k) number K221230. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the TRON?

TRON is a medical device that received FDA 510(k) clearance on 2022-07-28. The listed applicant is Xoran Technologies, LLC. The 510(k) number is K221230.

When did TRON receive FDA 510(k) clearance?

TRON received FDA 510(k) clearance on 2022-07-28, under 510(k) number K221230.

Who is the listed applicant for TRON?

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 TRON?

The FDA product code for TRON is OWB.

其他以 Xoran Technologies, LLC 為申請人之記錄

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。

K210257Xoran工作站，型號10050 K201825迷你CAT 2D

相關器械（代碼：OWB）

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。

K253726uAngio AVIVA CXShanghai United Imaging Healthcare Co., Ltd.K261413EXTRON 3;EXTRON 6DRTECH Corporation K254205Zenition 30Philips Medical Systems Nederland B.V.K260607防護系統（西門子 30x40）Radiaction , Ltd.K253670SmartCT (R3.0 (L10))Philips Medical Systems B.V.K252735C-beamPulmera, Inc.

官方來源

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