FDA 510(k)

Dose+（1.0）

K 號：K250064 · 2025-09-04

決定日期2025-09-04

產品代碼MUJ

諮詢委員會RA

決定相當於

器材摘要

Dose+ (1.0) is the device name listed in this FDA 510(k) record. The listed applicant is Mvision AI OY. It received FDA 510(k) clearance on 2025-09-04 under 510(k) number K250064. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Dose+ (1.0)?

Dose+ (1.0) is a medical device that received FDA 510(k) clearance on 2025-09-04. The listed applicant is Mvision AI OY. The 510(k) number is K250064.

When did Dose+ (1.0) receive FDA 510(k) clearance?

Dose+ (1.0) received FDA 510(k) clearance on 2025-09-04, under 510(k) number K250064.

Who is the listed applicant for Dose+ (1.0)?

The FDA 510(k) record lists Mvision AI OY as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dose+ (1.0)?

The FDA product code for Dose+ (1.0) is MUJ.

其他以 Mvision AI OY 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。

K241490Contour+ (MVision AI 分割)

相關器械（代碼：MUJ）

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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