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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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15 records meeting your search criteria returned- Product Code: MXC Product Problem: Application Program Version or Upgrade Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) CONFIRM 01/07/2020
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) CONFIRM 11/26/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) CONFIRM 11/26/2019
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) CONFIRM 10/17/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) CONFIRM 08/14/2019
ABBOTT CONFIRM 07/26/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) CONFIRM 06/10/2019
ABBOTT CONFIRM 06/07/2019
ABBOTT CRM CONFIRM 05/30/2019
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) CONFIRM 05/23/2019
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