RejuvatoneMD
K 號：K152199 · 2016-03-23
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器材摘要
RejuvatoneMD is the device name listed in this FDA 510(k) record. The listed applicant is Trophy Skin, Inc.. It received FDA 510(k) clearance on 2016-03-23 under 510(k) number K152199. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the RejuvatoneMD?
RejuvatoneMD is a medical device that received FDA 510(k) clearance on 2016-03-23. The listed applicant is Trophy Skin, Inc.. The 510(k) number is K152199.
When did RejuvatoneMD receive FDA 510(k) clearance?
RejuvatoneMD received FDA 510(k) clearance on 2016-03-23, under 510(k) number K152199.
Who is the listed applicant for RejuvatoneMD?
The FDA 510(k) record lists Trophy Skin, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RejuvatoneMD?
The FDA product code for RejuvatoneMD is NFO.
相關臨床試驗
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相關器械（代碼：NFO）
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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