Motive™ 腰部肌肉刺激器 (OT01-1003)
K 號：K253478 · 2025-11-06
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器材摘要
Motive™ Muscle Stimulator for Lower Back (OT01-1003) is the device name listed in this FDA 510(k) record. The listed applicant is Motive Health, Inc.. It received FDA 510(k) clearance on 2025-11-06 under 510(k) number K253478. 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 Motive™ Muscle Stimulator for Lower Back (OT01-1003)?
Motive™ Muscle Stimulator for Lower Back (OT01-1003) is a medical device that received FDA 510(k) clearance on 2025-11-06. The listed applicant is Motive Health, Inc.. The 510(k) number is K253478.
When did Motive™ Muscle Stimulator for Lower Back (OT01-1003) receive FDA 510(k) clearance?
Motive™ Muscle Stimulator for Lower Back (OT01-1003) received FDA 510(k) clearance on 2025-11-06, under 510(k) number K253478.
Who is the listed applicant for Motive™ Muscle Stimulator for Lower Back (OT01-1003)?
The FDA 510(k) record lists Motive Health, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Motive™ Muscle Stimulator for Lower Back (OT01-1003)?
The FDA product code for Motive™ Muscle Stimulator for Lower Back (OT01-1003) is NGX.
相關臨床試驗
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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
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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