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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
TOSHIBA AMERICA MEDICAL SYSTEMS CORPORAT TOSHIBA 12/21/2015
PHILIPS HEALTHCARE PHILIPS DIAGNOST 96 11/04/2015
WSO GE MEDICAL SYSTEMS, LLC PRECISION 500D 11/01/2015
WSO GE MEDICAL SYSTEMS, LLC PRECISION 500D 10/20/2015
SIEMENS GMBH AXIOM ICONOS R200 10/13/2015
SIEMENS AG/SIEMENS HEALTHCARE GMBH SIEMENS LUMINOS AGILE SYSTEM 10/01/2015
UNKNOWN GE 09/17/2015
GE OEC MEDICAL SYSTEMS (SLC) 6800 08/13/2015
GE OEC MEDICAL SYSTEMS 9900 08/12/2015
GE OEC MEDICAL SYSTEMS 9800 08/12/2015
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