產生器，衝擊波，用於疼痛緩解
PMA 核准號：P080028 · 2020-02-05
廣告
器材摘要
Generator, shock-wave, for pain relief is the device name listed in this FDA 510(k) record. The listed applicant is Storz Medical AG. It received FDA 510(k) clearance on 2020-02-05. The device is classified under product code NBN. It was reviewed by the SU advisory panel.
常見問題
What is the Generator, shock-wave, for pain relief?
Generator, shock-wave, for pain relief is a medical device that received FDA 510(k) clearance on 2020-02-05. The listed applicant is Storz Medical AG.
When did Generator, shock-wave, for pain relief receive FDA 510(k) clearance?
The clearance date for Generator, shock-wave, for pain relief can be found in the official FDA records.
Who is the listed applicant for Generator, shock-wave, for pain relief?
The FDA 510(k) record lists Storz Medical AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Generator, shock-wave, for pain relief?
The FDA product code for Generator, shock-wave, for pain relief is NBN.
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