FDA 510(k)

C&B陶瓷；C&B永久；C&B臨時

K 號：K233273 · 2024-11-27

決定日期2024-11-27

產品代碼EBF

諮詢委員會DE

決定相當於

器材摘要

C&B Ceramic; C&B Permanent; C&B Interim is the device name listed in this FDA 510(k) record. The listed applicant is Prevest Denpro Limited. It received FDA 510(k) clearance on 2024-11-27 under 510(k) number K233273. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the C&B Ceramic; C&B Permanent; C&B Interim?

C&B Ceramic; C&B Permanent; C&B Interim is a medical device that received FDA 510(k) clearance on 2024-11-27. The listed applicant is Prevest Denpro Limited. The 510(k) number is K233273.

When did C&B Ceramic; C&B Permanent; C&B Interim receive FDA 510(k) clearance?

C&B Ceramic; C&B Permanent; C&B Interim received FDA 510(k) clearance on 2024-11-27, under 510(k) number K233273.

Who is the listed applicant for C&B Ceramic; C&B Permanent; C&B Interim?

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

What is the FDA product code for C&B Ceramic; C&B Permanent; C&B Interim?

The FDA product code for C&B Ceramic; C&B Permanent; C&B Interim is EBF.

其他以 Prevest Denpro Limited 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：EBF）

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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