LiVac 復位器系統
K 號：K162445 · 2016-10-20
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器材摘要
LiVac Retractor System is the device name listed in this FDA 510(k) record. The listed applicant is Livac Pty, Ltd.. It received FDA 510(k) clearance on 2016-10-20 under 510(k) number K162445. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LiVac Retractor System?
LiVac Retractor System is a medical device that received FDA 510(k) clearance on 2016-10-20. The listed applicant is Livac Pty, Ltd.. The 510(k) number is K162445.
When did LiVac Retractor System receive FDA 510(k) clearance?
LiVac Retractor System received FDA 510(k) clearance on 2016-10-20, under 510(k) number K162445.
Who is the listed applicant for LiVac Retractor System?
The FDA 510(k) record lists Livac Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LiVac Retractor System?
The FDA product code for LiVac Retractor System is GCJ.
相關臨床試驗
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相關器械（代碼：GCJ）
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
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