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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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123 records meeting your search criteria returned- Product Code: LWS Product Problem: Difficult to Interrogate Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) CURRENT DR RF 04/14/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) CURRENT DR RF 03/16/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) FORTIFY DR, U1.6 SJ4 ID 03/16/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) FORTIFY ST DR, U1.6 DF1 ID 03/11/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) ELLIPSE DR ICD, US 03/02/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) FORTIFY ASSURA DR ICD, US 01/31/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) FORTIFY VR, U1.6 SJ4 US 01/26/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) FORTIFY ASSURA DR ICD, US 01/26/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) ELLIPSE VR ICD, US 01/10/2017
ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE) FORTIFY DR, U1.6 SJ4 US 12/27/2016
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