FDA 510(k)

LIFEPAK® 35 AC電源适配器 (41335-000001)

K 號：K240162 · 2024-04-19

決定日期2024-04-19

產品代碼MPD

諮詢委員會履歷

決定相當於

器材摘要

LIFEPAK® 35 AC Power Adapter (41335-000001) is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Physio-Control. It received FDA 510(k) clearance on 2024-04-19 under 510(k) number K240162. The device is classified under product code MPD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LIFEPAK® 35 AC Power Adapter (41335-000001)?

LIFEPAK® 35 AC Power Adapter (41335-000001) is a medical device that received FDA 510(k) clearance on 2024-04-19. The listed applicant is Stryker Physio-Control. The 510(k) number is K240162.

When did LIFEPAK® 35 AC Power Adapter (41335-000001) receive FDA 510(k) clearance?

LIFEPAK® 35 AC Power Adapter (41335-000001) received FDA 510(k) clearance on 2024-04-19, under 510(k) number K240162.

Who is the listed applicant for LIFEPAK® 35 AC Power Adapter (41335-000001)?

The FDA 510(k) record lists Stryker Physio-Control as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFEPAK® 35 AC Power Adapter (41335-000001)?

The FDA product code for LIFEPAK® 35 AC Power Adapter (41335-000001) is MPD.

其他以 Stryker Physio-Control 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。

K240377LIFEPAK® 心電圖電纜

相關器械（代碼：MPD）

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。

K253099LIFEPAK 15 AC電源适配器（41577-000333）Physio-Control, Inc.

官方來源

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