FDA 510(k)

MIM - 百分位數等級量表

K 號：K233620 · 2024-05-20

決定日期2024-05-20

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

MIM - Centiloid Scaling 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 2024-05-20 under 510(k) number K233620. 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 - Centiloid Scaling?

MIM - Centiloid Scaling is a medical device that received FDA 510(k) clearance on 2024-05-20. The listed applicant is Mim Software, Inc.. The 510(k) number is K233620.

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

MIM - Centiloid Scaling received FDA 510(k) clearance on 2024-05-20, under 510(k) number K233620.

Who is the listed applicant for MIM - Centiloid Scaling?

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 - Centiloid Scaling?

The FDA product code for MIM - Centiloid Scaling 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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