JBS-LVO
K 號：K241480 · 2024-09-27
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器材摘要
JBS-LVO is the device name listed in this FDA 510(k) record. The listed applicant is JLK, Inc.. It received FDA 510(k) clearance on 2024-09-27 under 510(k) number K241480. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the JBS-LVO?
JBS-LVO is a medical device that received FDA 510(k) clearance on 2024-09-27. The listed applicant is JLK, Inc.. The 510(k) number is K241480.
When did JBS-LVO receive FDA 510(k) clearance?
JBS-LVO received FDA 510(k) clearance on 2024-09-27, under 510(k) number K241480.
Who is the listed applicant for JBS-LVO?
The FDA 510(k) record lists JLK, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JBS-LVO?
The FDA product code for JBS-LVO is QAS.
其他以 JLK, Inc. 為申請人之記錄
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相關器械（代碼：QAS）
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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