FDA 510(k)

Sentimag 系統

K 號：K222832 · 2023-01-21

決定日期2023-01-21

產品代碼NEU

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Sentimag System is the device name listed in this FDA 510(k) record. The listed applicant is Endomagnetics Ltd.,. It received FDA 510(k) clearance on 2023-01-21 under 510(k) number K222832. The device is classified under product code NEU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sentimag System?

Sentimag System is a medical device that received FDA 510(k) clearance on 2023-01-21. The listed applicant is Endomagnetics Ltd.,. The 510(k) number is K222832.

When did Sentimag System receive FDA 510(k) clearance?

Sentimag System received FDA 510(k) clearance on 2023-01-21, under 510(k) number K222832.

Who is the listed applicant for Sentimag System?

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

What is the FDA product code for Sentimag System?

The FDA product code for Sentimag System is NEU.

其他以 Endomagnetics 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。

K232865磁種Pro磁標記系統 K173587磁種磁標記系統 K163541磁種磁標記系統 K153044Sentimag系統，Sentimark磁標記系統

相關器械（代碼：NEU）

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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