免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

貝爾澤 MPS® (UW機器灌流解決方案) (BMPS-001)

K 號:K243840 · 2025-03-26

決定日期2025-03-26
產品代碼KDN
諮詢委員會GU
決定相當於

器材摘要

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) is the device name listed in this FDA 510(k) record. The listed applicant is Bridge TO Life. It received FDA 510(k) clearance on 2025-03-26 under 510(k) number K243840. The device is classified under product code KDN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)?

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) is a medical device that received FDA 510(k) clearance on 2025-03-26. The listed applicant is Bridge TO Life. The 510(k) number is K243840.

When did Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) receive FDA 510(k) clearance?

Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) received FDA 510(k) clearance on 2025-03-26, under 510(k) number K243840.

Who is the listed applicant for Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)?

The FDA 510(k) record lists Bridge TO Life as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001)?

The FDA product code for Belzer MPS® (UW Machine Perfusion Solution) (BMPS-001) is KDN.

相關臨床試驗

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。

其他以 Bridge TO Life 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:KDN)

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

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。

↑