免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料，僅供一般參考，不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

ScandiDos Delta4 Discover，另名：ScandiDos Delta4 Discover+

K 號：K151426 · 2016-01-29

申請人Scandidos AB
決定日期2016-01-29
產品代碼IYE
諮詢委員會RA
決定相當於

器材摘要

ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ is the device name listed in this FDA 510(k) record. The listed applicant is Scandidos AB. It received FDA 510(k) clearance on 2016-01-29 under 510(k) number K151426. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+?

ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ is a medical device that received FDA 510(k) clearance on 2016-01-29. The listed applicant is Scandidos AB. The 510(k) number is K151426.

When did ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ receive FDA 510(k) clearance?

ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ received FDA 510(k) clearance on 2016-01-29, under 510(k) number K151426.

Who is the listed applicant for ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+?

The FDA 510(k) record lists Scandidos AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+?

The FDA product code for ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ is IYE.

相關臨床試驗

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。

NCT07608549FLASH 預試階段 1 安全性研究NOT_YET_RECRUITINGNCT06562205PAP系統外部臨床研究（ECS）NOT_YET_RECRUITINGNCT06443177對於動脈瘤性硬腦膜下出血引起的腦血管收縮，交感調節的影響SUSPENDEDNCT07095751人工智能協助的Uro-Cam導尿管評估系統，用於診斷膀胱癌NOT_YET_RECRUITING

其他以 Scandidos AB 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。

K223234Delta4洞察K183606Delta4 Phantom+ MR (PMMA), Delta4 Phantom+ MR (PW)

相關器械（代碼：IYE）

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。

K261865AerFrame™ 對齊雷射箱 (LBV2)Stabilix, LLCK261718EZFluence (RADEZ V2)Radformation, Inc.K260733MRIA 放射治療資訊系統 (MRIA)Manteia Technologies Co., Ltd.K261856Halcyon, Ethos 放射治療系統 (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser Applikationen

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。

↑