Tria Sapphire
K 號：K160821 · 2016-06-15
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器材摘要
Tria Sapphire is the device name listed in this FDA 510(k) record. The listed applicant is Tria Beauty, Inc.. It received FDA 510(k) clearance on 2016-06-15 under 510(k) number K160821. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Tria Sapphire?
Tria Sapphire is a medical device that received FDA 510(k) clearance on 2016-06-15. The listed applicant is Tria Beauty, Inc.. The 510(k) number is K160821.
When did Tria Sapphire receive FDA 510(k) clearance?
Tria Sapphire received FDA 510(k) clearance on 2016-06-15, under 510(k) number K160821.
Who is the listed applicant for Tria Sapphire?
The FDA 510(k) record lists Tria Beauty, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tria Sapphire?
The FDA product code for Tria Sapphire is OLP.
相關臨床試驗
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相關器械（代碼：OLP）
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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