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FDA 510(k)

牙科X光單元(AJX200)

K 號:K252110 · 2026-03-12

決定日期2026-03-12
產品代碼EHD
諮詢委員會DE
決定相當於

器材摘要

Dental X-RAY Unit (AJX200) is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Ajax Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2026-03-12 under 510(k) number K252110. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Dental X-RAY Unit (AJX200)?

Dental X-RAY Unit (AJX200) is a medical device that received FDA 510(k) clearance on 2026-03-12. The listed applicant is Guangzhou Ajax Medical Equipment Co., Ltd.. The 510(k) number is K252110.

When did Dental X-RAY Unit (AJX200) receive FDA 510(k) clearance?

Dental X-RAY Unit (AJX200) received FDA 510(k) clearance on 2026-03-12, under 510(k) number K252110.

Who is the listed applicant for Dental X-RAY Unit (AJX200)?

The FDA 510(k) record lists Guangzhou Ajax Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dental X-RAY Unit (AJX200)?

The FDA product code for Dental X-RAY Unit (AJX200) is EHD.

相關臨床試驗

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其他以 Guangzhou Ajax Medical Equipment 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。

相關器械(代碼:EHD)

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。

官方來源

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