• 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 
 > 
 
29 records meeting your search criteria returned- Product Code: LYJ Patient Problem: Aspiration/Inhalation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIVANOVA USA, INC. PULSE GEN MODEL 102 11/17/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 106 09/26/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 105 08/17/2023
LIVANOVA USA, INC. PULSE GEN MODEL 106 07/07/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 106 03/03/2023
CYBERONICS / LIVANOVA USA, INC. SENTIVA GENERATOR 12/30/2022
CYBERONICS - HOUSTON PULSE GEN MODEL 1000 12/27/2022
LIVANOVA USA, INC. LEAD MODEL 304 07/25/2022
LIVANOVA USA, INC. PULSE GEN MODEL 1000 05/03/2022
LIVANOVA USA, INC. PULSE GEN MODEL 106 04/12/2022
-
-