FDA 510(k)

OCS 心臟白血球濾過器

K 號：K231362 · 2023-10-31

決定日期2023-10-31

產品代碼DTM

諮詢委員會履歷

決定相當於

器材摘要

OCS Heart Leukocyte Depleting Filter is the device name listed in this FDA 510(k) record. The listed applicant is TransMedics, Inc.. It received FDA 510(k) clearance on 2023-10-31 under 510(k) number K231362. The device is classified under product code DTM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the OCS Heart Leukocyte Depleting Filter?

OCS Heart Leukocyte Depleting Filter is a medical device that received FDA 510(k) clearance on 2023-10-31. The listed applicant is TransMedics, Inc.. The 510(k) number is K231362.

When did OCS Heart Leukocyte Depleting Filter receive FDA 510(k) clearance?

OCS Heart Leukocyte Depleting Filter received FDA 510(k) clearance on 2023-10-31, under 510(k) number K231362.

Who is the listed applicant for OCS Heart Leukocyte Depleting Filter?

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

What is the FDA product code for OCS Heart Leukocyte Depleting Filter?

The FDA product code for OCS Heart Leukocyte Depleting Filter is DTM.

其他以 TransMedics, Inc. 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。

K222535OCS 肺臟捐贈者沖洗組合 K211314OCS 肺部解決方案

相關器械（代碼：DTM）

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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