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FDA 510(k)

先進皮膚更新設備

K 號：K182498 · 2018-11-30

申請人Jiangsu Unimed Laser Technology Co., Ltd.
決定日期2018-11-30
產品代碼ONG
諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。
決定相當於

器材摘要

Advanced Skin Renewing Device is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Unimed Laser Technology Co., Ltd.. It received FDA 510(k) clearance on 2018-11-30 under 510(k) number K182498. The device is classified under product code ONG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Advanced Skin Renewing Device?

Advanced Skin Renewing Device is a medical device that received FDA 510(k) clearance on 2018-11-30. The listed applicant is Jiangsu Unimed Laser Technology Co., Ltd.. The 510(k) number is K182498.

When did Advanced Skin Renewing Device receive FDA 510(k) clearance?

Advanced Skin Renewing Device received FDA 510(k) clearance on 2018-11-30, under 510(k) number K182498.

Who is the listed applicant for Advanced Skin Renewing Device?

The FDA 510(k) record lists Jiangsu Unimed Laser Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Advanced Skin Renewing Device?

The FDA product code for Advanced Skin Renewing Device is ONG.

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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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