FDA 510(k)

EasyOne 過濾器

K 號：K221250 · 2022-11-22

決定日期2022-11-22

產品代碼CAH

諮詢委員會AN

決定相當於

器材摘要

EasyOne Filter is the device name listed in this FDA 510(k) record. The listed applicant is Ndd Medizintechnik AG. It received FDA 510(k) clearance on 2022-11-22 under 510(k) number K221250. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the EasyOne Filter?

EasyOne Filter is a medical device that received FDA 510(k) clearance on 2022-11-22. The listed applicant is Ndd Medizintechnik AG. The 510(k) number is K221250.

When did EasyOne Filter receive FDA 510(k) clearance?

EasyOne Filter received FDA 510(k) clearance on 2022-11-22, under 510(k) number K221250.

Who is the listed applicant for EasyOne Filter?

The FDA 510(k) record lists Ndd Medizintechnik AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EasyOne Filter?

The FDA product code for EasyOne Filter is CAH.

其他以 Ndd Medizintechnik AG 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：CAH）

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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