FDA 510(k)

數位X光攝影系統（MobileApex 60E、MobileApex 60F、MobileApex 60G、MobileApex 60H）

K 號：K240284 · 2024-03-28

決定日期2024-03-28

產品代碼IZL

諮詢委員會RA

決定相當於

器材摘要

Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Browiner Tech Co., Ltd.. It received FDA 510(k) clearance on 2024-03-28 under 510(k) number K240284. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H)?

Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H) is a medical device that received FDA 510(k) clearance on 2024-03-28. The listed applicant is Shenzhen Browiner Tech Co., Ltd.. The 510(k) number is K240284.

When did Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H) receive FDA 510(k) clearance?

Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H) received FDA 510(k) clearance on 2024-03-28, under 510(k) number K240284.

Who is the listed applicant for Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H)?

The FDA 510(k) record lists Shenzhen Browiner Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H)?

The FDA product code for Digital Radiography System (MobileApex 60E, MobileApex 60F, MobileApex 60G, MobileApex 60H) is IZL.

其他以 Shenzhen Browiner Tech Co., Ltd. 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。

K240841數位X光攝影系統（ManntiX B，ManntiX K）

相關器械（代碼：IZL）

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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