FDA 510(k)

ESTELITE BULK FILL 流體

K 號：K161353 · 2017-04-03

決定日期2017-04-03

產品代碼EBF

諮詢委員會DE

決定相當於

器材摘要

ESTELITE BULK FILL Flow is the device name listed in this FDA 510(k) record. The listed applicant is Tokuyama Dental Corporation. It received FDA 510(k) clearance on 2017-04-03 under 510(k) number K161353. 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 ESTELITE BULK FILL Flow?

ESTELITE BULK FILL Flow is a medical device that received FDA 510(k) clearance on 2017-04-03. The listed applicant is Tokuyama Dental Corporation. The 510(k) number is K161353.

When did ESTELITE BULK FILL Flow receive FDA 510(k) clearance?

ESTELITE BULK FILL Flow received FDA 510(k) clearance on 2017-04-03, under 510(k) number K161353.

Who is the listed applicant for ESTELITE BULK FILL Flow?

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

What is the FDA product code for ESTELITE BULK FILL Flow?

The FDA product code for ESTELITE BULK FILL Flow is EBF.

其他以 Tokuyama Dental Corporation 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。

K262982Core·it雙用式醫療設備規範文本Spident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695流動性修復材質（KP-Flow LF，KP-Flow MF，KP-Flow HF）Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus 填充劑；Tetric plus 流動劑Ivoclar Vivadent, Inc.K262228超越大量填充濃縮複合材料Ultradent Products, Inc.K261246SRGC-06GC America, Inc.

官方來源

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