酸鹼，玻尿酸，關節內注射
PMA 核准號：P030019 · 2026-08-28
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器材摘要
Acid, hyaluronic, intraarticular is the device name listed in this FDA 510(k) record. The listed applicant is Anika Therapeutics, Inc.. It received FDA 510(k) clearance on 2026-08-28. The device is classified under product code MOZ. It was reviewed by the OR advisory panel.
常見問題
What is the Acid, hyaluronic, intraarticular?
Acid, hyaluronic, intraarticular is a medical device that received FDA 510(k) clearance on 2026-08-28. The listed applicant is Anika Therapeutics, Inc..
When did Acid, hyaluronic, intraarticular receive FDA 510(k) clearance?
The clearance date for Acid, hyaluronic, intraarticular can be found in the official FDA records.
誰是Acid, hyaluronic, intraarticular的列名申請人？
FDA 510(k) 記錄將Anika Therapeutics, Inc. 列為申請人。這並不單獨確立設備製造商。
FDA產品代碼為酸鹼、透明質酸、關節內注射的產品是什麼？
FDA產品代碼，酸鹼性、透明質酸、關節內注射產品為MOZ。
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。
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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