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FDA 510(k)

Indigo® 雷霆抽吸系統 – 選擇+™ 管子

K 號:K241399 · 2024-06-10

決定日期2024-06-10
產品代碼QEW
諮詢委員會履歷
決定相當於

器材摘要

Indigo® Lightning Flash Aspiration System – Select +™ Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Penumbra, Inc.. It received FDA 510(k) clearance on 2024-06-10 under 510(k) number K241399. The device is classified under product code QEW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Indigo® Lightning Flash Aspiration System – Select +™ Catheter?

Indigo® Lightning Flash Aspiration System – Select +™ Catheter is a medical device that received FDA 510(k) clearance on 2024-06-10. The listed applicant is Penumbra, Inc.. The 510(k) number is K241399.

When did Indigo® Lightning Flash Aspiration System – Select +™ Catheter receive FDA 510(k) clearance?

Indigo® Lightning Flash Aspiration System – Select +™ Catheter received FDA 510(k) clearance on 2024-06-10, under 510(k) number K241399.

Who is the listed applicant for Indigo® Lightning Flash Aspiration System – Select +™ Catheter?

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

What is the FDA product code for Indigo® Lightning Flash Aspiration System – Select +™ Catheter?

The FDA product code for Indigo® Lightning Flash Aspiration System – Select +™ Catheter is QEW.

相關臨床試驗

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其他以 Penumbra, Inc. 為申請人之記錄

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相關器械(代碼:QEW)

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

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