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FDA 510(k)

川澄多樣本適配器,配備預裝夾子(MBCH)

K 號:K223810 · 2023-02-24

決定日期2023-02-24
產品代碼JKA
諮詢委員會CH
決定相當於

器材摘要

Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH) is the device name listed in this FDA 510(k) record. The listed applicant is Sb-Kawasumi Laboratories, Inc.. It received FDA 510(k) clearance on 2023-02-24 under 510(k) number K223810. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH)?

Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH) is a medical device that received FDA 510(k) clearance on 2023-02-24. The listed applicant is Sb-Kawasumi Laboratories, Inc.. The 510(k) number is K223810.

When did Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH) receive FDA 510(k) clearance?

Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH) received FDA 510(k) clearance on 2023-02-24, under 510(k) number K223810.

Who is the listed applicant for Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH)?

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

What is the FDA product code for Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH)?

The FDA product code for Kawasumi Multiple Sample Adapter with Pre-Attached Holder (MBCH) is JKA.

相關臨床試驗

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其他以 Sb-Kawasumi Laboratories, Inc. 為申請人之記錄

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相關器械(代碼:JKA)

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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