TheraFace 微電流
K 號：K212238 · 2021-09-29
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器材摘要
TheraFace Microcurrent is the device name listed in this FDA 510(k) record. The listed applicant is Theragun, Inc.. It received FDA 510(k) clearance on 2021-09-29 under 510(k) number K212238. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TheraFace Microcurrent?
TheraFace Microcurrent is a medical device that received FDA 510(k) clearance on 2021-09-29. The listed applicant is Theragun, Inc.. The 510(k) number is K212238.
When did TheraFace Microcurrent receive FDA 510(k) clearance?
TheraFace Microcurrent received FDA 510(k) clearance on 2021-09-29, under 510(k) number K212238.
Who is the listed applicant for TheraFace Microcurrent?
The FDA 510(k) record lists Theragun, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TheraFace Microcurrent?
The FDA product code for TheraFace Microcurrent is NFO.
相關臨床試驗
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其他以 Theragun, Inc. 為申請人之記錄
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。
相關器械（代碼：NFO）
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。
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官方來源
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