FDA 510(k)

一次性血夾（AF系列）

K 號：K231633 · 2024-01-11

申請人Alton (Shanghai) Medical Instruments Co., Ltd.

決定日期2024-01-11

產品代碼PKL

諮詢委員會GU

決定相當於

器材摘要

Disposable Hemoclip (AF series) is the device name listed in this FDA 510(k) record. The listed applicant is Alton (Shanghai) Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2024-01-11 under 510(k) number K231633. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Disposable Hemoclip (AF series)?

Disposable Hemoclip (AF series) is a medical device that received FDA 510(k) clearance on 2024-01-11. The listed applicant is Alton (Shanghai) Medical Instruments Co., Ltd.. The 510(k) number is K231633.

When did Disposable Hemoclip (AF series) receive FDA 510(k) clearance?

Disposable Hemoclip (AF series) received FDA 510(k) clearance on 2024-01-11, under 510(k) number K231633.

Who is the listed applicant for Disposable Hemoclip (AF series)?

The FDA 510(k) record lists Alton (Shanghai) Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Hemoclip (AF series)?

The FDA product code for Disposable Hemoclip (AF series) is PKL.

其他以 Alton (Shanghai) Medical Instruments Co., 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。

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相關器械（代碼：PKL）

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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