CORGRIP NG/NI 管道固定系統
K 號：K162110 · 2016-09-15
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器材摘要
CORGRIP NG/NI Tube Retention System is the device name listed in this FDA 510(k) record. The listed applicant is Corpak Medsystems, Inc. A Division of Haylard Health. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K162110. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
常見問題
What is the CORGRIP NG/NI Tube Retention System?
CORGRIP NG/NI Tube Retention System is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Corpak Medsystems, Inc. A Division of Haylard Health. The 510(k) number is K162110.
When did CORGRIP NG/NI Tube Retention System receive FDA 510(k) clearance?
CORGRIP NG/NI Tube Retention System received FDA 510(k) clearance on 2016-09-15, under 510(k) number K162110.
Who is the listed applicant for CORGRIP NG/NI Tube Retention System?
The FDA 510(k) record lists Corpak Medsystems, Inc. A Division of Haylard Health as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CORGRIP NG/NI Tube Retention System?
The FDA product code for CORGRIP NG/NI Tube Retention System is KNT.
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相關器械（代碼：KNT）
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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