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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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4 records meeting your search criteria returned- Product Code: OWB Product Problem: Improper Device Output Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE GMBH ARTIS ZEEGO 10/20/2017
GE MEDICAL SYSTEMS SCS INNOVA 2000 01/26/2017
PHILIPS HEALTHCARE ALLURA XPER FD20 BIPLANE 10/26/2015
GE MEDICAL SYSTEMS SCS INNOVA 2000 01/17/2014
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