FDA 510(k)

3M® ActiV.A.C.® 罐 - 300ml 含凝胶 (M8275058/5, M8275058/10)

K 號：K241134 · 2024-05-23

決定日期2024-05-23

產品代碼OMP

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10) is the device name listed in this FDA 510(k) record. The listed applicant is Kci USA, Inc.. It received FDA 510(k) clearance on 2024-05-23 under 510(k) number K241134. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the 3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10)?

3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10) is a medical device that received FDA 510(k) clearance on 2024-05-23. The listed applicant is Kci USA, Inc.. The 510(k) number is K241134.

When did 3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10) receive FDA 510(k) clearance?

3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10) received FDA 510(k) clearance on 2024-05-23, under 510(k) number K241134.

Who is the listed applicant for 3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10)?

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

What is the FDA product code for 3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10)?

The FDA product code for 3M™ ActiV.A.C.™ Canister - 300ml with Gel (M8275058/5, M8275058/10) is OMP.

其他以 Kci USA, Inc. 為申請人之記錄

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相關器械（代碼：OMP）

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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