健身帶（型號：KLT-07）
K 號：K231136 · 2023-06-16
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器材摘要
Fitness Belt (Model: KLT-07) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Kelutongda Industrial Co., Ltd.. It received FDA 510(k) clearance on 2023-06-16 under 510(k) number K231136. 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 Fitness Belt (Model: KLT-07)?
Fitness Belt (Model: KLT-07) is a medical device that received FDA 510(k) clearance on 2023-06-16. The listed applicant is Shenzhen Kelutongda Industrial Co., Ltd.. The 510(k) number is K231136.
When did Fitness Belt (Model: KLT-07) receive FDA 510(k) clearance?
Fitness Belt (Model: KLT-07) received FDA 510(k) clearance on 2023-06-16, under 510(k) number K231136.
Who is the listed applicant for Fitness Belt (Model: KLT-07)?
The FDA 510(k) record lists Shenzhen Kelutongda Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Fitness Belt (Model: KLT-07)?
The FDA product code for Fitness Belt (Model: KLT-07) 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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