Laport
K 號：K171741 · 2017-08-29
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器材摘要
Laport is the device name listed in this FDA 510(k) record. The listed applicant is Sejong Medical Co., Ltd.. It received FDA 510(k) clearance on 2017-08-29 under 510(k) number K171741. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Laport?
Laport is a medical device that received FDA 510(k) clearance on 2017-08-29. The listed applicant is Sejong Medical Co., Ltd.. The 510(k) number is K171741.
When did Laport receive FDA 510(k) clearance?
Laport received FDA 510(k) clearance on 2017-08-29, under 510(k) number K171741.
Who is the listed applicant for Laport?
The FDA 510(k) record lists Sejong Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Laport?
The FDA product code for Laport is GCJ.
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其他以 Sejong Medical Co., Ltd. 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：GCJ）
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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