FDA 510(k)平面LED配對
K 號:K230362 · 2023-09-11
決定日期2023-09-11
產品代碼OHT
諮詢委員會SU
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決定相當於
器材摘要
Planar LED mate is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Leaflife Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-09-11 under 510(k) number K230362. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Planar LED mate?
Planar LED mate is a medical device that received FDA 510(k) clearance on 2023-09-11. The listed applicant is Shenzhen Leaflife Technology Co., Ltd.. The 510(k) number is K230362.
When did Planar LED mate receive FDA 510(k) clearance?
Planar LED mate received FDA 510(k) clearance on 2023-09-11, under 510(k) number K230362.
Who is the listed applicant for Planar LED mate?
The FDA 510(k) record lists Shenzhen Leaflife Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Planar LED mate?
The FDA product code for Planar LED mate is OHT.
相關臨床試驗
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。
其他以 Shenzhen Leaflife Technology Co., Ltd. 為申請人之記錄
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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相關器械(代碼:OHT)
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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