我的觸肌電刺激器
K 號：K233098 · 2024-08-02
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器材摘要
MYOTouch Muscle Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Sunmed, LLC. It received FDA 510(k) clearance on 2024-08-02 under 510(k) number K233098. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MYOTouch Muscle Stimulator?
MYOTouch Muscle Stimulator is a medical device that received FDA 510(k) clearance on 2024-08-02. The listed applicant is Sunmed, LLC. The 510(k) number is K233098.
When did MYOTouch Muscle Stimulator receive FDA 510(k) clearance?
MYOTouch Muscle Stimulator received FDA 510(k) clearance on 2024-08-02, under 510(k) number K233098.
Who is the listed applicant for MYOTouch Muscle Stimulator?
The FDA 510(k) record lists Sunmed, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MYOTouch Muscle Stimulator?
The FDA product code for MYOTouch Muscle Stimulator is IPF.
相關臨床試驗
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相關器械（代碼：IPF）
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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