LM-9300 Plus 鑫石碎機
K 號：K213772 · 2023-01-19
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器材摘要
LM-9300 Plus Lithotripter is the device name listed in this FDA 510(k) record. The listed applicant is Lite-Med, Inc.. It received FDA 510(k) clearance on 2023-01-19 under 510(k) number K213772. The device is classified under product code LNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LM-9300 Plus Lithotripter?
LM-9300 Plus Lithotripter is a medical device that received FDA 510(k) clearance on 2023-01-19. The listed applicant is Lite-Med, Inc.. The 510(k) number is K213772.
When did LM-9300 Plus Lithotripter receive FDA 510(k) clearance?
LM-9300 Plus Lithotripter received FDA 510(k) clearance on 2023-01-19, under 510(k) number K213772.
Who is the listed applicant for LM-9300 Plus Lithotripter?
The FDA 510(k) record lists Lite-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LM-9300 Plus Lithotripter?
The FDA product code for LM-9300 Plus Lithotripter is LNS.
相關臨床試驗
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相關器械（代碼：LNS）
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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