刺激器，骨生長，非侵入式
PMA 核准號：P850022 · 2024-02-29
廣告
器材摘要
Stimulator, bone growth, non-invasive is the device name listed in this FDA 510(k) record. The listed applicant is Ahp Eos Buyer, Inc.. It received FDA 510(k) clearance on 2024-02-29. The device is classified under product code LOF. It was reviewed by the OR advisory panel.
常見問題
What is the Stimulator, bone growth, non-invasive?
Stimulator, bone growth, non-invasive is a medical device that received FDA 510(k) clearance on 2024-02-29. The listed applicant is Ahp Eos Buyer, Inc..
When did Stimulator, bone growth, non-invasive receive FDA 510(k) clearance?
The clearance date for Stimulator, bone growth, non-invasive can be found in the official FDA records.
Who is the listed applicant for Stimulator, bone growth, non-invasive?
The FDA 510(k) record lists Ahp Eos Buyer, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stimulator, bone growth, non-invasive?
The FDA product code for Stimulator, bone growth, non-invasive is LOF.
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。
廣告