FastFit電肌肉刺激系統
K 號：K192161 · 2020-01-22
廣告
器材摘要
FastFit EMS System is the device name listed in this FDA 510(k) record. The listed applicant is Fast Fit, LLC. It received FDA 510(k) clearance on 2020-01-22 under 510(k) number K192161. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the FastFit EMS System?
FastFit EMS System is a medical device that received FDA 510(k) clearance on 2020-01-22. The listed applicant is Fast Fit, LLC. The 510(k) number is K192161.
When did FastFit EMS System receive FDA 510(k) clearance?
FastFit EMS System received FDA 510(k) clearance on 2020-01-22, under 510(k) number K192161.
Who is the listed applicant for FastFit EMS System?
The FDA 510(k) record lists Fast Fit, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FastFit EMS System?
The FDA product code for FastFit EMS System is NGX.
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相關器械（代碼：NGX）
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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