再製超扭力及超扭力加強診斷血管內視鏡針
K 號：K231015 · 2024-07-01
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器材摘要
常見問題
What is the Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?
Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters is a medical device that received FDA 510(k) clearance on 2024-07-01. The listed applicant is Innovative Health, LLC. The 510(k) number is K231015.
When did Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters receive FDA 510(k) clearance?
Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters received FDA 510(k) clearance on 2024-07-01, under 510(k) number K231015.
Who is the listed applicant for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?
The FDA 510(k) record lists Innovative Health, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?
The FDA product code for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters is NLI.
相關臨床試驗
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其他以 Innovative Health, LLC 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。
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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