LeEject 2 齿科注射器和針系統
K 號：K171254 · 2017-11-16
廣告
器材摘要
LeEject 2 Dental Syringe and Needle System is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Technology and Capital, Inc.. It received FDA 510(k) clearance on 2017-11-16 under 510(k) number K171254. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LeEject 2 Dental Syringe and Needle System?
LeEject 2 Dental Syringe and Needle System is a medical device that received FDA 510(k) clearance on 2017-11-16. The listed applicant is Advanced Technology and Capital, Inc.. The 510(k) number is K171254.
When did LeEject 2 Dental Syringe and Needle System receive FDA 510(k) clearance?
LeEject 2 Dental Syringe and Needle System received FDA 510(k) clearance on 2017-11-16, under 510(k) number K171254.
Who is the listed applicant for LeEject 2 Dental Syringe and Needle System?
The FDA 510(k) record lists Advanced Technology and Capital, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LeEject 2 Dental Syringe and Needle System?
The FDA product code for LeEject 2 Dental Syringe and Needle System is EJI.
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。
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。
廣告