ASSISTO 大眾應用器夾具裝置
K 號：K201279 · 2020-07-10
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器材摘要
ASSISTO Universal Applicator Clamping Device is the device name listed in this FDA 510(k) record. The listed applicant is Geomed Medizin-Technik GmbH & Co. KG. It received FDA 510(k) clearance on 2020-07-10 under 510(k) number K201279. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ASSISTO Universal Applicator Clamping Device?
ASSISTO Universal Applicator Clamping Device is a medical device that received FDA 510(k) clearance on 2020-07-10. The listed applicant is Geomed Medizin-Technik GmbH & Co. KG. The 510(k) number is K201279.
When did ASSISTO Universal Applicator Clamping Device receive FDA 510(k) clearance?
ASSISTO Universal Applicator Clamping Device received FDA 510(k) clearance on 2020-07-10, under 510(k) number K201279.
Who is the listed applicant for ASSISTO Universal Applicator Clamping Device?
The FDA 510(k) record lists Geomed Medizin-Technik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASSISTO Universal Applicator Clamping Device?
The FDA product code for ASSISTO Universal Applicator Clamping Device is JAQ.
相關臨床試驗
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相關器械（代碼：JAQ）
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
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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