LOUIS系列4強化剪，LOUIS系列5
K 號：K221102 · 2022-12-15
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器材摘要
LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is the device name listed in this FDA 510(k) record. The listed applicant is Sra Developments, Ltd.. It received FDA 510(k) clearance on 2022-12-15 under 510(k) number K221102. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.
常見問題
What is the LOTUS Series 4 Enhanced Shears, LOTUS Series 5?
LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is a medical device that received FDA 510(k) clearance on 2022-12-15. The listed applicant is Sra Developments, Ltd.. The 510(k) number is K221102.
When did LOTUS Series 4 Enhanced Shears, LOTUS Series 5 receive FDA 510(k) clearance?
LOTUS Series 4 Enhanced Shears, LOTUS Series 5 received FDA 510(k) clearance on 2022-12-15, under 510(k) number K221102.
Who is the listed applicant for LOTUS Series 4 Enhanced Shears, LOTUS Series 5?
The FDA 510(k) record lists Sra Developments, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOTUS Series 4 Enhanced Shears, LOTUS Series 5?
The FDA product code for LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is LFL.
相關臨床試驗
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相關器械（代碼：LFL）
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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