FDA 510(k)

Aveir 回收导管

K 號：K213494 · 2022-04-01

決定日期2022-04-01

產品代碼MMX

諮詢委員會履歷

決定相當於

器材摘要

Aveir Retrieval Catheter is the device name listed in this FDA 510(k) record. The listed applicant is ABBOTT MEDICAL. It received FDA 510(k) clearance on 2022-04-01 under 510(k) number K213494. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Aveir Retrieval Catheter?

Aveir Retrieval Catheter is a medical device that received FDA 510(k) clearance on 2022-04-01. The listed applicant is ABBOTT MEDICAL. The 510(k) number is K213494.

When did Aveir Retrieval Catheter receive FDA 510(k) clearance?

Aveir Retrieval Catheter received FDA 510(k) clearance on 2022-04-01, under 510(k) number K213494.

Who is the listed applicant for Aveir Retrieval Catheter?

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

What is the FDA product code for Aveir Retrieval Catheter?

The FDA product code for Aveir Retrieval Catheter is MMX.

其他以 ABBOTT MEDICAL 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：MMX）

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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