AirSculpt身形雕塑系統(AIRS-1-SYS)
K 號：K241835 · 2024-11-27
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器材摘要
AirSculpt Body Contouring System (AIRS-1-SYS) is the device name listed in this FDA 510(k) record. The listed applicant is Cellmyx. It received FDA 510(k) clearance on 2024-11-27 under 510(k) number K241835. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the AirSculpt Body Contouring System (AIRS-1-SYS)?
AirSculpt Body Contouring System (AIRS-1-SYS) is a medical device that received FDA 510(k) clearance on 2024-11-27. The listed applicant is Cellmyx. The 510(k) number is K241835.
When did AirSculpt Body Contouring System (AIRS-1-SYS) receive FDA 510(k) clearance?
AirSculpt Body Contouring System (AIRS-1-SYS) received FDA 510(k) clearance on 2024-11-27, under 510(k) number K241835.
Who is the listed applicant for AirSculpt Body Contouring System (AIRS-1-SYS)?
The FDA 510(k) record lists Cellmyx as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AirSculpt Body Contouring System (AIRS-1-SYS)?
The FDA product code for AirSculpt Body Contouring System (AIRS-1-SYS) is QPB.
相關臨床試驗
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相關器械（代碼：QPB）
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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