FDA 510(k)

tmCMF解決方案

K 號：K233874 · 2024-07-11

決定日期2024-07-11

產品代碼JEY

諮詢委員會DE

決定相當於

器材摘要

tmCMF Solution is the device name listed in this FDA 510(k) record. The listed applicant is Techmah Cmf. It received FDA 510(k) clearance on 2024-07-11 under 510(k) number K233874. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the tmCMF Solution?

tmCMF Solution is a medical device that received FDA 510(k) clearance on 2024-07-11. The listed applicant is Techmah Cmf. The 510(k) number is K233874.

When did tmCMF Solution receive FDA 510(k) clearance?

tmCMF Solution received FDA 510(k) clearance on 2024-07-11, under 510(k) number K233874.

Who is the listed applicant for tmCMF Solution?

The FDA 510(k) record lists Techmah Cmf as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for tmCMF Solution?

The FDA product code for tmCMF Solution is JEY.

其他以 Techmah Cmf 為申請人之記錄

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K231520tmCMF解決方案

相關器械（代碼：JEY）

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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