Kisses Plus 假牙系統
K 號：K172630 · 2018-04-03
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器材摘要
Kisses Plus Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Achimhai Medical Corporation. It received FDA 510(k) clearance on 2018-04-03 under 510(k) number K172630. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Kisses Plus Implant System?
Kisses Plus Implant System is a medical device that received FDA 510(k) clearance on 2018-04-03. The listed applicant is Achimhai Medical Corporation. The 510(k) number is K172630.
When did Kisses Plus Implant System receive FDA 510(k) clearance?
Kisses Plus Implant System received FDA 510(k) clearance on 2018-04-03, under 510(k) number K172630.
Who is the listed applicant for Kisses Plus Implant System?
The FDA 510(k) record lists Achimhai Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kisses Plus Implant System?
The FDA product code for Kisses Plus Implant System is DZE.
相關臨床試驗
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其他以 Achimhai Medical 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：DZE）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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