定義雷射微針治療系統
K 號：K232301 · 2024-03-14
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器材摘要
Define RF Microneedling System is the device name listed in this FDA 510(k) record. The listed applicant is Aesthetic Management Partners. It received FDA 510(k) clearance on 2024-03-14 under 510(k) number K232301. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Define RF Microneedling System?
Define RF Microneedling System is a medical device that received FDA 510(k) clearance on 2024-03-14. The listed applicant is Aesthetic Management Partners. The 510(k) number is K232301.
When did Define RF Microneedling System receive FDA 510(k) clearance?
Define RF Microneedling System received FDA 510(k) clearance on 2024-03-14, under 510(k) number K232301.
Who is the listed applicant for Define RF Microneedling System?
The FDA 510(k) record lists Aesthetic Management Partners as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Define RF Microneedling System?
The FDA product code for Define RF Microneedling System is GEI.
相關臨床試驗
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相關器械（代碼：GEI）
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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