牙科疼痛消除器
K 號：K182947 · 2019-03-26
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器材摘要
Dental Pain Eraser is the device name listed in this FDA 510(k) record. The listed applicant is Synapse Dental, LLC. It received FDA 510(k) clearance on 2019-03-26 under 510(k) number K182947. The device is classified under product code LWM. FDA Decision: Substantially Equivalent.
常見問題
What is the Dental Pain Eraser?
Dental Pain Eraser is a medical device that received FDA 510(k) clearance on 2019-03-26. The listed applicant is Synapse Dental, LLC. The 510(k) number is K182947.
When did Dental Pain Eraser receive FDA 510(k) clearance?
Dental Pain Eraser received FDA 510(k) clearance on 2019-03-26, under 510(k) number K182947.
Who is the listed applicant for Dental Pain Eraser?
The FDA 510(k) record lists Synapse Dental, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dental Pain Eraser?
The FDA product code for Dental Pain Eraser is LWM.
相關臨床試驗
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相關器械（代碼：LWM）
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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