Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
294 records meeting your search criteria returned- Product Code: LYJ Product Problem: Mechanical Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIVANOVA USA, INC. LEAD MODEL 302 02/04/2021
LIVANOVA USA, INC. PULSE GEN MODEL 1000 01/11/2021
LIVANOVA USA, INC. LEAD MODEL 304 01/11/2021
LIVANOVA USA, INC. LEAD MODEL 304 01/05/2021
LIVANOVA USA, INC. PULSE GEN MODEL 1000 12/29/2020
LIVANOVA USA, INC. LEAD MODEL 304 12/21/2020
LIVANOVA USA, INC. BIPOL LEAD MODEL 300 12/12/2020
LIVANOVA USA, INC. PULSE GEN MODEL 1000 12/04/2020
LIVANOVA USA, INC. LEAD MODEL 302 11/13/2020
LIVANOVA USA, INC. PULSE GEN MODEL 1000 11/10/2020
-
-