植入式，內胃囊用於病態肥胖
PMA 核准號：P180024 · 2019-04-16
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器材摘要
IMPLANT, INTRAGASTRIC FOR MORBID OBESITY is the device name listed in this FDA 510(k) record. The listed applicant is Baronova, Inc.. It received FDA 510(k) clearance on 2019-04-16. The device is classified under product code LTI. It was reviewed by the GU advisory panel.
常見問題
What is the IMPLANT, INTRAGASTRIC FOR MORBID OBESITY?
IMPLANT, INTRAGASTRIC FOR MORBID OBESITY is a medical device that received FDA 510(k) clearance on 2019-04-16. The listed applicant is Baronova, Inc..
When did IMPLANT, INTRAGASTRIC FOR MORBID OBESITY receive FDA 510(k) clearance?
The clearance date for IMPLANT, INTRAGASTRIC FOR MORBID OBESITY can be found in the official FDA records.
誰是IMPLANT, INTRAGASTRIC FOR MORBID OBESITY的列名申請人？
The FDA 510(k) record lists Baronova, Inc. as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼為IMPLANT, INTRAGASTRIC FOR MORBID OBESITY是什麼？
FDA產品代碼對於治療嚴重肥胖的內胃植入式設備為LTI。
相關臨床試驗
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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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