LV Liberty Vision 模型 1 90 鈾同位素近端放射源
K 號：K163572 · 2017-03-15
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器材摘要
LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source is the device name listed in this FDA 510(k) record. The listed applicant is Lv Liberty Vision Corp.. It received FDA 510(k) clearance on 2017-03-15 under 510(k) number K163572. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source?
LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source is a medical device that received FDA 510(k) clearance on 2017-03-15. The listed applicant is Lv Liberty Vision Corp.. The 510(k) number is K163572.
When did LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source receive FDA 510(k) clearance?
LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source received FDA 510(k) clearance on 2017-03-15, under 510(k) number K163572.
Who is the listed applicant for LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source?
The FDA 510(k) record lists Lv Liberty Vision Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source?
The FDA product code for LV Liberty Vision Model 1 90 Yttrium Brachytherapy Source is KXK.
相關臨床試驗
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相關器械（代碼：KXK）
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
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