精靈除毛雷射系列
K 號：K153718 · 2016-02-12
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器材摘要
Spirit Hair Removal laser Family is the device name listed in this FDA 510(k) record. The listed applicant is Active Optical Systems , Ltd.. It received FDA 510(k) clearance on 2016-02-12 under 510(k) number K153718. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常見問題
What is the Spirit Hair Removal laser Family?
Spirit Hair Removal laser Family is a medical device that received FDA 510(k) clearance on 2016-02-12. The listed applicant is Active Optical Systems , Ltd.. The 510(k) number is K153718.
When did Spirit Hair Removal laser Family receive FDA 510(k) clearance?
Spirit Hair Removal laser Family received FDA 510(k) clearance on 2016-02-12, under 510(k) number K153718.
Who is the listed applicant for Spirit Hair Removal laser Family?
The FDA 510(k) record lists Active Optical Systems , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spirit Hair Removal laser Family?
The FDA product code for Spirit Hair Removal laser Family is GEX. This falls under the Gastroenterology category.
相關臨床試驗
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相關器械（代碼：GEX）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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