Medax 結構切片系統 III
K 號：K181803 · 2018-10-18
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器材摘要
Medax Biopsy Systems III is the device name listed in this FDA 510(k) record. The listed applicant is Medax Srl Unipersonale. It received FDA 510(k) clearance on 2018-10-18 under 510(k) number K181803. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Medax Biopsy Systems III?
Medax Biopsy Systems III is a medical device that received FDA 510(k) clearance on 2018-10-18. The listed applicant is Medax Srl Unipersonale. The 510(k) number is K181803.
When did Medax Biopsy Systems III receive FDA 510(k) clearance?
Medax Biopsy Systems III received FDA 510(k) clearance on 2018-10-18, under 510(k) number K181803.
Who is the listed applicant for Medax Biopsy Systems III?
The FDA 510(k) record lists Medax Srl Unipersonale as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Medax Biopsy Systems III?
The FDA product code for Medax Biopsy Systems III is KNW.
相關臨床試驗
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其他以 Medax Srl Unipersonale 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：KNW）
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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