FDA 510(k)

MIM-Ablation

K号: K220256 · 2022-10-07

决定日期2022-10-07

产品代码QTZ

咨询委员会RA

决定实质等同

器械摘要

MIM-Ablation is the device name listed in this FDA 510(k) record. The listed applicant is Mim Software, Inc.. It received FDA 510(k) clearance on 2022-10-07 under 510(k) number K220256. The device is classified under product code QTZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MIM-Ablation?

MIM-Ablation is a medical device that received FDA 510(k) clearance on 2022-10-07. The listed applicant is Mim Software, Inc.. The 510(k) number is K220256.

When did MIM-Ablation receive FDA 510(k) clearance?

MIM-Ablation received FDA 510(k) clearance on 2022-10-07, under 510(k) number K220256.

Who is the listed applicant for MIM-Ablation?

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

What is the FDA product code for MIM-Ablation?

The FDA product code for MIM-Ablation is QTZ.

列明Mim Software, 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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