米雷特抓取器，鰍魚，米雷特抓取器，馬里蘭
K 號：K160149 · 2016-08-30
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器材摘要
Miret Grasper, Alligator, Miret Grasper, Maryland is the device name listed in this FDA 510(k) record. The listed applicant is Miret Surgical, Inc.. It received FDA 510(k) clearance on 2016-08-30 under 510(k) number K160149. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Miret Grasper, Alligator, Miret Grasper, Maryland?
Miret Grasper, Alligator, Miret Grasper, Maryland is a medical device that received FDA 510(k) clearance on 2016-08-30. The listed applicant is Miret Surgical, Inc.. The 510(k) number is K160149.
When did Miret Grasper, Alligator, Miret Grasper, Maryland receive FDA 510(k) clearance?
Miret Grasper, Alligator, Miret Grasper, Maryland received FDA 510(k) clearance on 2016-08-30, under 510(k) number K160149.
Who is the listed applicant for Miret Grasper, Alligator, Miret Grasper, Maryland?
The FDA 510(k) record lists Miret Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Miret Grasper, Alligator, Miret Grasper, Maryland?
The FDA product code for Miret Grasper, Alligator, Miret Grasper, Maryland is OCW.
相關臨床試驗
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：OCW）
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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