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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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76 records meeting your search criteria returned- Product Code: KNQ Product Problem: Detachment Of Device Component Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CORDIS DE MEXICO MAXI LD 7F 18X6 80CM 11/21/2016
BOSTON SCIENTIFIC - GALWAY XXL¿ ESOPHAGEAL 11/16/2016
BOSTON SCIENTIFIC - GALWAY XXL¿ ESOPHAGEAL 10/17/2016
BOSTON SCIENTIFIC - CORK CRE¿ FIXED WIRE 10/13/2016
BOSTON SCIENTIFIC - GALWAY XXL¿ VASCULAR 08/18/2016
BOSTON SCIENTIFIC - GALWAY XXL¿ ESOPHAGEAL 08/03/2016
BOSTON SCIENTIFIC - CORK CRE¿ WIREGUIDED 08/03/2016
BOSTON SCIENTIFIC - CORK CRE¿ WIREGUIDED 07/05/2016
BOSTON SCIENTIFIC - CORK CRE¿ WIREGUIDED 06/02/2016
CONMED CORPORATION MARKED SPRING TIP GUIDEWIRE 05/11/2016
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