FDA 510(k)

超密封XT plus - 豐比奧生物保護，超密封XT hydro - 豐比奧生物保護

K 號：K232498 · 2023-08-18

決定日期2023-08-18

產品代碼EBC

諮詢委員會DE

決定相當於

器材摘要

UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio is the device name listed in this FDA 510(k) record. The listed applicant is Ultradent Product, Inc.. It received FDA 510(k) clearance on 2023-08-18 under 510(k) number K232498. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio?

UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio is a medical device that received FDA 510(k) clearance on 2023-08-18. The listed applicant is Ultradent Product, Inc.. The 510(k) number is K232498.

When did UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio receive FDA 510(k) clearance?

UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio received FDA 510(k) clearance on 2023-08-18, under 510(k) number K232498.

Who is the listed applicant for UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio?

The FDA 510(k) record lists Ultradent Product, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio?

The FDA product code for UltraSeal XT plus - Bioprotection by Nobio, UltraSeal XT hydro - Bioprotection by Nobio is EBC.

其他以 Ultradent Product, Inc. 為申請人之記錄

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K201795超越

相關器械（代碼：EBC）

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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