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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
BOSTON SCIENTIFIC - CORK CRE¿ FIXED WIRE 03/31/2017
BOSTON SCIENTIFIC - CORK CRE¿ WIREGUIDED 03/27/2017
BOSTON SCIENTIFIC - COSTA RICA (COYOL) CRE PRO GI 03/13/2017
BOSTON SCIENTIFIC - COSTA RICA (COYOL) CRE PRO GI 03/08/2017
BOSTON SCIENTIFIC - GALWAY XXL¿ ESOPHAGEAL 02/14/2017
BOSTON SCIENTIFIC - CORK CRE¿ WIREGUIDED 01/18/2017
BOSTON SCIENTIFIC - CORK CRE¿ WIREGUIDED 12/30/2016
BOSTON SCIENTIFIC - GALWAY XXL¿ ESOPHAGEAL 12/16/2016
BOSTON SCIENTIFIC - CORK CRE PRO GI 11/30/2016
BOSTON SCIENTIFIC - CORK CRE PRO GI 11/23/2016
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