系統、雷射、光纖、光動治療
PMA 核准號：P940010 · 2021-02-24
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決定日期2021-02-24
PMA 編號P940010
產品代碼MVG
器械分類3 類
醫療專科U
諮詢委員會SU
請提供完整的描述文本，以便我進行翻譯。
器材摘要
System, laser, fiber optic, photodynamic therapy is the device name listed in this FDA 510(k) record. The listed applicant is Pinnacle Biologics, Inc.. It received FDA 510(k) clearance on 2021-02-24. The device is classified under product code MVG. It was reviewed by the SU advisory panel.
常見問題
What is the System, laser, fiber optic, photodynamic therapy?
System, laser, fiber optic, photodynamic therapy is a medical device that received FDA 510(k) clearance on 2021-02-24. The listed applicant is Pinnacle Biologics, Inc..
When did System, laser, fiber optic, photodynamic therapy receive FDA 510(k) clearance?
The clearance date for System, laser, fiber optic, photodynamic therapy can be found in the official FDA records.
Who is the listed applicant for System, laser, fiber optic, photodynamic therapy?
The FDA 510(k) record lists Pinnacle Biologics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for System, laser, fiber optic, photodynamic therapy?
The FDA product code for System, laser, fiber optic, photodynamic therapy is MVG.
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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