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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.
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ManufacturerBrand NameDate Report Received
CYBERONICS - HOUSTON LEAD MODEL 302 09/29/2017
CYBERONICS - HOUSTON LEAD MODEL 302 09/29/2017
CYBERONICS - HOUSTON PULSE GEN MODEL 106 09/29/2017
CYBERONICS - HOUSTON PULSE GEN MODEL 106 09/29/2017
CYBERONICS - HOUSTON PULSE GEN MODEL 105 09/29/2017
CYBERONICS - HOUSTON PULSE GEN MODEL 106 09/29/2017
CYBERONICS - HOUSTON PULSE GEN MODEL 106 09/29/2017
CYBERONICS - HOUSTON PULSE GEN MODEL 106 09/29/2017
CYBERONICS - HOUSTON LEAD MODEL 303 09/28/2017
CYBERONICS - HOUSTON PULSE GEN MODEL 106 09/28/2017
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