AS軟體版本Asera
K 號：K260205 · 2026-02-19
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器材摘要
AS Software Version Asera is the device name listed in this FDA 510(k) record. The listed applicant is AS Software, LLC. It received FDA 510(k) clearance on 2026-02-19 under 510(k) number K260205. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the AS Software Version Asera?
AS Software Version Asera is a medical device that received FDA 510(k) clearance on 2026-02-19. The listed applicant is AS Software, LLC. The 510(k) number is K260205.
When did AS Software Version Asera receive FDA 510(k) clearance?
AS Software Version Asera received FDA 510(k) clearance on 2026-02-19, under 510(k) number K260205.
Who is the listed applicant for AS Software Version Asera?
The FDA 510(k) record lists AS Software, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AS Software Version Asera?
The FDA product code for AS Software Version Asera is LLZ.
相關臨床試驗
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相關器械（代碼：LLZ）
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。
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