OGYILI TENS/NMES 刺激器
K 號：K201431 · 2020-11-09
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器材摘要
OGYILI TENS/NMES Stimulator is the device name listed in this FDA 510(k) record. The listed applicant is Gongguan Tutamen Metalwork Co., Ltd.. It received FDA 510(k) clearance on 2020-11-09 under 510(k) number K201431. 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 OGYILI TENS/NMES Stimulator?
OGYILI TENS/NMES Stimulator is a medical device that received FDA 510(k) clearance on 2020-11-09. The listed applicant is Gongguan Tutamen Metalwork Co., Ltd.. The 510(k) number is K201431.
When did OGYILI TENS/NMES Stimulator receive FDA 510(k) clearance?
OGYILI TENS/NMES Stimulator received FDA 510(k) clearance on 2020-11-09, under 510(k) number K201431.
Who is the listed applicant for OGYILI TENS/NMES Stimulator?
The FDA 510(k) record lists Gongguan Tutamen Metalwork Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OGYILI TENS/NMES Stimulator?
The FDA product code for OGYILI TENS/NMES Stimulator 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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