膀胱掃描器型號：BVT02
K 號：K223448 · 2023-07-07
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器材摘要
Bladder Scanner Model: BVT02 is the device name listed in this FDA 510(k) record. The listed applicant is Xuzhou Kaixin Electronic Instrument Co., Ltd.. It received FDA 510(k) clearance on 2023-07-07 under 510(k) number K223448. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Bladder Scanner Model: BVT02?
Bladder Scanner Model: BVT02 is a medical device that received FDA 510(k) clearance on 2023-07-07. The listed applicant is Xuzhou Kaixin Electronic Instrument Co., Ltd.. The 510(k) number is K223448.
When did Bladder Scanner Model: BVT02 receive FDA 510(k) clearance?
Bladder Scanner Model: BVT02 received FDA 510(k) clearance on 2023-07-07, under 510(k) number K223448.
Who is the listed applicant for Bladder Scanner Model: BVT02?
The FDA 510(k) record lists Xuzhou Kaixin Electronic Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bladder Scanner Model: BVT02?
The FDA product code for Bladder Scanner Model: BVT02 is IYO.
相關臨床試驗
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相關器械（代碼：IYO）
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。
官方來源
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