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FDA 510(k)

Pulpdent (Activa) 齿溝裂縫填充劑含MCP

K 號:K172169 · 2018-01-05

決定日期2018-01-05
產品代碼EBC
諮詢委員會DE
決定相當於

器材摘要

Pulpdent (Activa) Pit and Fissure Sealant with MCP is the device name listed in this FDA 510(k) record. The listed applicant is Pulpdent Corporation. It received FDA 510(k) clearance on 2018-01-05 under 510(k) number K172169. 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 Pulpdent (Activa) Pit and Fissure Sealant with MCP?

Pulpdent (Activa) Pit and Fissure Sealant with MCP is a medical device that received FDA 510(k) clearance on 2018-01-05. The listed applicant is Pulpdent Corporation. The 510(k) number is K172169.

When did Pulpdent (Activa) Pit and Fissure Sealant with MCP receive FDA 510(k) clearance?

Pulpdent (Activa) Pit and Fissure Sealant with MCP received FDA 510(k) clearance on 2018-01-05, under 510(k) number K172169.

Who is the listed applicant for Pulpdent (Activa) Pit and Fissure Sealant with MCP?

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

What is the FDA product code for Pulpdent (Activa) Pit and Fissure Sealant with MCP?

The FDA product code for Pulpdent (Activa) Pit and Fissure Sealant with MCP is EBC.

相關臨床試驗

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。

其他以 Pulpdent 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。

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。

官方來源

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