潘羅拉X-ERA PF/NF/MF
K 號：K182198 · 2019-01-31
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器材摘要
Panoura X-ERA PF/NF/MF is the device name listed in this FDA 510(k) record. The listed applicant is The Yoshida Dental Mfg. Co., Ltd.. It received FDA 510(k) clearance on 2019-01-31 under 510(k) number K182198. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Panoura X-ERA PF/NF/MF?
Panoura X-ERA PF/NF/MF is a medical device that received FDA 510(k) clearance on 2019-01-31. The listed applicant is The Yoshida Dental Mfg. Co., Ltd.. The 510(k) number is K182198.
When did Panoura X-ERA PF/NF/MF receive FDA 510(k) clearance?
Panoura X-ERA PF/NF/MF received FDA 510(k) clearance on 2019-01-31, under 510(k) number K182198.
Who is the listed applicant for Panoura X-ERA PF/NF/MF?
The FDA 510(k) record lists The Yoshida Dental Mfg. Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Panoura X-ERA PF/NF/MF?
The FDA product code for Panoura X-ERA PF/NF/MF is MUH.
相關臨床試驗
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相關器械（代碼：MUH）
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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