N7-S
K 號:K240168 · 2024-09-12
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器材摘要
N7-S is the device name listed in this FDA 510(k) record. The listed applicant is Nuga Medical Co., Ltd.. It received FDA 510(k) clearance on 2024-09-12 under 510(k) number K240168. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the N7-S?
N7-S is a medical device that received FDA 510(k) clearance on 2024-09-12. The listed applicant is Nuga Medical Co., Ltd.. The 510(k) number is K240168.
When did N7-S receive FDA 510(k) clearance?
N7-S received FDA 510(k) clearance on 2024-09-12, under 510(k) number K240168.
Who is the listed applicant for N7-S?
The FDA 510(k) record lists Nuga Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for N7-S?
The FDA product code for N7-S is JFB.
其他以 Nuga Medical Co., Ltd. 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:JFB)
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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