NobleStitch EL
K 號：K162617 · 2017-04-06
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決定日期2017-04-06
產品代碼GAW
諮詢委員會SU
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決定Unknown
器材摘要
NobleStitch EL is the device name listed in this FDA 510(k) record. The listed applicant is Nobles Medical Technologies Ii, Inc.. It received FDA 510(k) clearance on 2017-04-06 under 510(k) number K162617. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Unknown.
常見問題
What is the NobleStitch EL?
NobleStitch EL is a medical device that received FDA 510(k) clearance on 2017-04-06. The listed applicant is Nobles Medical Technologies Ii, Inc.. The 510(k) number is K162617.
When did NobleStitch EL receive FDA 510(k) clearance?
NobleStitch EL received FDA 510(k) clearance on 2017-04-06, under 510(k) number K162617.
Who is the listed applicant for NobleStitch EL?
The FDA 510(k) record lists Nobles Medical Technologies Ii, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NobleStitch EL?
The FDA product code for NobleStitch EL is GAW.
相關臨床試驗
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相關器械（代碼：GAW）
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
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