Avid IF2
K 號：K183692 · 2019-06-12
廣告
決定日期2019-06-12
產品代碼LIH
諮詢委員會NE
(請提供完整的英文描述，以便進行翻譯。)
決定相當於
器材摘要
Avid IF2 is the device name listed in this FDA 510(k) record. The listed applicant is Vision Quest Industries Inc./Dba VQ Orthocare. It received FDA 510(k) clearance on 2019-06-12 under 510(k) number K183692. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Avid IF2?
Avid IF2 is a medical device that received FDA 510(k) clearance on 2019-06-12. The listed applicant is Vision Quest Industries Inc./Dba VQ Orthocare. The 510(k) number is K183692.
When did Avid IF2 receive FDA 510(k) clearance?
Avid IF2 received FDA 510(k) clearance on 2019-06-12, under 510(k) number K183692.
Who is the listed applicant for Avid IF2?
The FDA 510(k) record lists Vision Quest Industries Inc./Dba VQ Orthocare as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Avid IF2?
The FDA product code for Avid IF2 is LIH.
其他以 Vision Quest Industries Inc./Dba VQ Orthocare 為申請人之記錄
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相關器械（代碼：LIH）
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。
廣告