iRelieve 微電流疼痛緩解系統
K 號：K212618 · 2022-09-14
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器材摘要
iRelieve Microcurrent Pain Relief System is the device name listed in this FDA 510(k) record. The listed applicant is Fast Track Technologies, Inc.. It received FDA 510(k) clearance on 2022-09-14 under 510(k) number K212618. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the iRelieve Microcurrent Pain Relief System?
iRelieve Microcurrent Pain Relief System is a medical device that received FDA 510(k) clearance on 2022-09-14. The listed applicant is Fast Track Technologies, Inc.. The 510(k) number is K212618.
When did iRelieve Microcurrent Pain Relief System receive FDA 510(k) clearance?
iRelieve Microcurrent Pain Relief System received FDA 510(k) clearance on 2022-09-14, under 510(k) number K212618.
Who is the listed applicant for iRelieve Microcurrent Pain Relief System?
The FDA 510(k) record lists Fast Track Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iRelieve Microcurrent Pain Relief System?
The FDA product code for iRelieve Microcurrent Pain Relief System is GZJ.
相關臨床試驗
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相關器械（代碼：GZJ）
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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