Lariat, 熱/冷圈
K 號：K200745 · 2020-04-21
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器材摘要
Lariat, Hot/Cold Snare is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 2020-04-21 under 510(k) number K200745. The device is classified under product code FDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Lariat, Hot/Cold Snare?
Lariat, Hot/Cold Snare is a medical device that received FDA 510(k) clearance on 2020-04-21. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K200745.
When did Lariat, Hot/Cold Snare receive FDA 510(k) clearance?
Lariat, Hot/Cold Snare received FDA 510(k) clearance on 2020-04-21, under 510(k) number K200745.
Who is the listed applicant for Lariat, Hot/Cold Snare?
The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lariat, Hot/Cold Snare?
The FDA product code for Lariat, Hot/Cold Snare is FDI.
相關臨床試驗
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其他以 United States Endoscopy Group, Inc. 為申請人之記錄
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。
相關器械（代碼：FDI）
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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