OrthoView 7.2
K 號：K171068 · 2017-10-18
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器材摘要
OrthoView 7.2 is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Technique, Ltd.. It received FDA 510(k) clearance on 2017-10-18 under 510(k) number K171068. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the OrthoView 7.2?
OrthoView 7.2 is a medical device that received FDA 510(k) clearance on 2017-10-18. The listed applicant is Meridian Technique, Ltd.. The 510(k) number is K171068.
When did OrthoView 7.2 receive FDA 510(k) clearance?
OrthoView 7.2 received FDA 510(k) clearance on 2017-10-18, under 510(k) number K171068.
Who is the listed applicant for OrthoView 7.2?
The FDA 510(k) record lists Meridian Technique, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OrthoView 7.2?
The FDA product code for OrthoView 7.2 is LLZ.
相關臨床試驗
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相關器械（代碼：LLZ）
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。
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