威金斯醫療外科儀器
K 號：K200383 · 2020-07-21
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器材摘要
Wiggins Medical Surgical Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Wiggins Medical. It received FDA 510(k) clearance on 2020-07-21 under 510(k) number K200383. The device is classified under product code HAE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Wiggins Medical Surgical Instruments?
Wiggins Medical Surgical Instruments is a medical device that received FDA 510(k) clearance on 2020-07-21. The listed applicant is Wiggins Medical. The 510(k) number is K200383.
When did Wiggins Medical Surgical Instruments receive FDA 510(k) clearance?
Wiggins Medical Surgical Instruments received FDA 510(k) clearance on 2020-07-21, under 510(k) number K200383.
Who is the listed applicant for Wiggins Medical Surgical Instruments?
The FDA 510(k) record lists Wiggins Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Wiggins Medical Surgical Instruments?
The FDA product code for Wiggins Medical Surgical Instruments is HAE.
相關臨床試驗
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相關器械（代碼：HAE）
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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