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FDA 510(k)

NOMAD Pro 3

K 號:K253864 · 2026-03-20

決定日期2026-03-20
產品代碼EHD
諮詢委員會DE
決定相當於

器材摘要

NOMAD Pro 3 is the device name listed in this FDA 510(k) record. The listed applicant is Dental Imaging Technologies Corporation. It received FDA 510(k) clearance on 2026-03-20 under 510(k) number K253864. 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 NOMAD Pro 3?

NOMAD Pro 3 is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Dental Imaging Technologies Corporation. The 510(k) number is K253864.

When did NOMAD Pro 3 receive FDA 510(k) clearance?

NOMAD Pro 3 received FDA 510(k) clearance on 2026-03-20, under 510(k) number K253864.

Who is the listed applicant for NOMAD Pro 3?

The FDA 510(k) record lists Dental Imaging Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOMAD Pro 3?

The FDA product code for NOMAD Pro 3 is EHD.

相關臨床試驗

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其他以 Dental Imaging Technologies Corporation 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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