MINE
K 號：K180671 · 2019-06-05
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器材摘要
MINE is the device name listed in this FDA 510(k) record. The listed applicant is Rht Co., Ltd.. It received FDA 510(k) clearance on 2019-06-05 under 510(k) number K180671. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MINE?
MINE is a medical device that received FDA 510(k) clearance on 2019-06-05. The listed applicant is Rht Co., Ltd.. The 510(k) number is K180671.
When did MINE receive FDA 510(k) clearance?
MINE received FDA 510(k) clearance on 2019-06-05, under 510(k) number K180671.
Who is the listed applicant for MINE?
The FDA 510(k) record lists Rht Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINE?
The FDA product code for MINE is EHD.
相關 PubMed 文獻
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相關器械（代碼：EHD）
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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