FDA 510(k)

Ventripoint醫療系統 Plus (VMS+) 4.0

K 號：K241222 · 2025-02-26

決定日期2025-02-26

產品代碼QIH

諮詢委員會RA

決定相當於

器材摘要

Ventripoint Medical System Plus (VMS+) 4.0 is the device name listed in this FDA 510(k) record. The listed applicant is Ventripoint Diagnostics , Ltd.. It received FDA 510(k) clearance on 2025-02-26 under 510(k) number K241222. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Ventripoint Medical System Plus (VMS+) 4.0?

Ventripoint Medical System Plus (VMS+) 4.0 is a medical device that received FDA 510(k) clearance on 2025-02-26. The listed applicant is Ventripoint Diagnostics , Ltd.. The 510(k) number is K241222.

When did Ventripoint Medical System Plus (VMS+) 4.0 receive FDA 510(k) clearance?

Ventripoint Medical System Plus (VMS+) 4.0 received FDA 510(k) clearance on 2025-02-26, under 510(k) number K241222.

Who is the listed applicant for Ventripoint Medical System Plus (VMS+) 4.0?

The FDA 510(k) record lists Ventripoint Diagnostics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ventripoint Medical System Plus (VMS+) 4.0?

The FDA product code for Ventripoint Medical System Plus (VMS+) 4.0 is QIH.

其他以 Ventripoint Diagnostics , 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。

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相關器械（代碼：QIH）

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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