FDA 510(k)

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

K号: K241134 · 2024-05-23

决定日期2024-05-23

产品代码OMP

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决定实质等同

器械摘要

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.

常见问题

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.

列明Kci USA, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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官方来源

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数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。