• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 
 
30 records meeting your search criteria returned- Product Code: LYJ Patient Problem: Edema Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIVANOVA USA, INC. PULSE GEN MODEL 1000 04/30/2019
LIVANOVA USA, INC. PULSE GEN MODEL 105 04/26/2019
LIVANOVA USA, INC. LEAD MODEL 304 04/02/2019
LIVANOVA USA, INC. LEAD MODEL 304 03/29/2019
CYBERONICS - HOUSTON LEAD MODEL 304 03/19/2019
LIVANOVA USA, INC. PULSE GEN MODEL 106 03/04/2019
LIVANOVA USA, INC. PULSE GEN MODEL 106 02/08/2019
LIVANOVA USA, INC. PULSE GEN MODEL 1000 01/23/2019
LIVANOVA USA, INC. PULSE GEN MODEL 1000 01/14/2019
LIVANOVA USA, INC. PULSE GEN MODEL 106 01/03/2019
-
-