Device, thermal ablation, endometrial
PMA 核准號：P970021 · 2016-01-04
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器材摘要
Device, thermal ablation, endometrial is the device name listed in this FDA 510(k) record. The listed applicant is Gynecare, Inc.. It received FDA 510(k) clearance on 2016-01-04. The device is classified under product code MNB. It was reviewed by the OB advisory panel.
常見問題
What is the Device, thermal ablation, endometrial?
Device, thermal ablation, endometrial is a medical device that received FDA 510(k) clearance on 2016-01-04. The listed applicant is Gynecare, Inc..
When did Device, thermal ablation, endometrial receive FDA 510(k) clearance?
The clearance date for Device, thermal ablation, endometrial can be found in the official FDA records.
Who is the listed applicant for Device, thermal ablation, endometrial?
The FDA 510(k) record lists Gynecare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Device, thermal ablation, endometrial?
The FDA product code for Device, thermal ablation, endometrial is MNB.
相關臨床試驗
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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