8ch T/R 髋膝螺線管
K 號：K223225 · 2023-02-14
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器材摘要
8ch T/R Knee Coil is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen RF Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-02-14 under 510(k) number K223225. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the 8ch T/R Knee Coil?
8ch T/R Knee Coil is a medical device that received FDA 510(k) clearance on 2023-02-14. The listed applicant is Shenzhen RF Tech Co., Ltd.. The 510(k) number is K223225.
When did 8ch T/R Knee Coil receive FDA 510(k) clearance?
8ch T/R Knee Coil received FDA 510(k) clearance on 2023-02-14, under 510(k) number K223225.
Who is the listed applicant for 8ch T/R Knee Coil?
The FDA 510(k) record lists Shenzhen RF Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 8ch T/R Knee Coil?
The FDA product code for 8ch T/R Knee Coil is MOS.
其他以 Shenzhen RF Tech Co., Ltd. 為申請人之記錄
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相關器械（代碼：MOS）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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