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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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87 records meeting your search criteria returned- Product Code: DXE Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC FETCH 2 ASPIRATION CATHETER 05/12/2015
PENUMBRA, INC. INDIGO SYSTEM CAT3 ASPIRATION CATHETER 04/01/2015
PENUMBRA, INC. INDIGO SYSTEM SEPARATOR 5 03/06/2015
PENUMBRA, INC. INDIGO SYSTEM SEPARATOR 5 12/19/2014
PENUMBRA, INC. INDIGO SYSTEM SEPARATOR 5 11/07/2014
MICRUS ENDOVASCULAR, LLC REVIVE - THROMBECTOMY DEVICE 09/10/2014
MICRUS ENDOVASCULAR, LLC REVIVE - THROMBECTOMY DEVICE 09/10/2014
MICRUS ENDOVASCULAR, LLC REVIVE - THROMBECTOMY DEVICE 09/10/2014
MICRUS ENDOVASCULAR, LLC REVIVE - THROMBECTOMY DEVICE 09/10/2014
MICRUS ENDOVASCULAR, LLC REVIVE - THROMBECTOMY DEVICE 09/10/2014
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