dS足踝I6CH 1.5T線圈
K 號：K162177 · 2016-09-14
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器材摘要
dS FootAnkle I6CH 1.5T Coil is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation. It received FDA 510(k) clearance on 2016-09-14 under 510(k) number K162177. 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 dS FootAnkle I6CH 1.5T Coil?
dS FootAnkle I6CH 1.5T Coil is a medical device that received FDA 510(k) clearance on 2016-09-14. The listed applicant is Invivo Corporation. The 510(k) number is K162177.
When did dS FootAnkle I6CH 1.5T Coil receive FDA 510(k) clearance?
dS FootAnkle I6CH 1.5T Coil received FDA 510(k) clearance on 2016-09-14, under 510(k) number K162177.
Who is the listed applicant for dS FootAnkle I6CH 1.5T Coil?
The FDA 510(k) record lists Invivo Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for dS FootAnkle I6CH 1.5T Coil?
The FDA product code for dS FootAnkle I6CH 1.5T Coil is MOS.
相關臨床試驗
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其他以 Invivo Corporation 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。
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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