脂保儲
K 號：K212969 · 2024-08-07
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器材摘要
Liposaver is the device name listed in this FDA 510(k) record. The listed applicant is Lhbiomed Co., Ltd.. It received FDA 510(k) clearance on 2024-08-07 under 510(k) number K212969. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Liposaver?
Liposaver is a medical device that received FDA 510(k) clearance on 2024-08-07. The listed applicant is Lhbiomed Co., Ltd.. The 510(k) number is K212969.
When did Liposaver receive FDA 510(k) clearance?
Liposaver received FDA 510(k) clearance on 2024-08-07, under 510(k) number K212969.
Who is the listed applicant for Liposaver?
The FDA 510(k) record lists Lhbiomed Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Liposaver?
The FDA product code for Liposaver is QPB.
相關臨床試驗
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相關器械（代碼：QPB）
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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