FDA 510(k)

預先密封劑

K 號：K161580 · 2016-10-18

決定日期2016-10-18

產品代碼EBC

諮詢委員會DE

決定相當於

器材摘要

Premier Sealant is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Company Products. It received FDA 510(k) clearance on 2016-10-18 under 510(k) number K161580. 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 Premier Sealant?

Premier Sealant is a medical device that received FDA 510(k) clearance on 2016-10-18. The listed applicant is Premier Dental Company Products. The 510(k) number is K161580.

When did Premier Sealant receive FDA 510(k) clearance?

Premier Sealant received FDA 510(k) clearance on 2016-10-18, under 510(k) number K161580.

Who is the listed applicant for Premier Sealant?

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

What is the FDA product code for Premier Sealant?

The FDA product code for Premier Sealant is EBC.

其他以 Premier Dental Company Products 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。

K180682AeroPro 離線預防系統

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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官方來源

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