FDA 510(k)

C.C. Life 21

K 號：K230459 · 2023-10-19

決定日期2023-10-19

產品代碼NFO

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

C.C. Life 21 is the device name listed in this FDA 510(k) record. The listed applicant is 21 Equipment S.R.L.. It received FDA 510(k) clearance on 2023-10-19 under 510(k) number K230459. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the C.C. Life 21?

C.C. Life 21 is a medical device that received FDA 510(k) clearance on 2023-10-19. The listed applicant is 21 Equipment S.R.L.. The 510(k) number is K230459.

When did C.C. Life 21 receive FDA 510(k) clearance?

C.C. Life 21 received FDA 510(k) clearance on 2023-10-19, under 510(k) number K230459.

Who is the listed applicant for C.C. Life 21?

The FDA 510(k) record lists 21 Equipment S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C.C. Life 21?

The FDA product code for C.C. Life 21 is NFO.

其他以 21 Equipment S.R.L. 為申請人之記錄

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K213295C.C. LIFE 21

相關器械（代碼：NFO）

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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