FDA 510(k)

MIM – 剂量分析

K 號：K232514 · 2024-05-06

決定日期2024-05-06

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

MIM – Dose Analysis 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 2024-05-06 under 510(k) number K232514. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MIM – Dose Analysis?

MIM – Dose Analysis is a medical device that received FDA 510(k) clearance on 2024-05-06. The listed applicant is Mim Software, Inc.. The 510(k) number is K232514.

When did MIM – Dose Analysis receive FDA 510(k) clearance?

MIM – Dose Analysis received FDA 510(k) clearance on 2024-05-06, under 510(k) number K232514.

Who is the listed applicant for MIM – Dose Analysis?

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 – Dose Analysis?

The FDA product code for MIM – Dose Analysis is LLZ.

其他以 Mim Software, Inc. 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：LLZ）

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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