Delight, Delight正骨科, B&Lite S
K 號：K170529 · 2017-08-08
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器材摘要
Delight, Delight ortho, B&Lite S is the device name listed in this FDA 510(k) record. The listed applicant is Dentall Co., Ltd.. It received FDA 510(k) clearance on 2017-08-08 under 510(k) number K170529. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Delight, Delight ortho, B&Lite S?
Delight, Delight ortho, B&Lite S is a medical device that received FDA 510(k) clearance on 2017-08-08. The listed applicant is Dentall Co., Ltd.. The 510(k) number is K170529.
When did Delight, Delight ortho, B&Lite S receive FDA 510(k) clearance?
Delight, Delight ortho, B&Lite S received FDA 510(k) clearance on 2017-08-08, under 510(k) number K170529.
Who is the listed applicant for Delight, Delight ortho, B&Lite S?
The FDA 510(k) record lists Dentall Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Delight, Delight ortho, B&Lite S?
The FDA product code for Delight, Delight ortho, B&Lite S is EBZ.
相關臨床試驗
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相關器械（代碼：EBZ）
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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