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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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5 records meeting your search criteria returned- Product Code: DQO Patient Problem: Unspecified Infection Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDTRONIC, INC DXTERITY TRA 02/24/2020
CORDIS CASHEL 466P306X 06/08/2018
CORDIS CASHEL UNKNOWN TRAPEASE VENA CAVA FILTER. 04/16/2018
NAVILYST MEDICAL NAVILYST MEDICAL / XCELA 04/23/2014
CPI - DEL CARIBE ENDOTAK RELIANCE 01/17/2014
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