• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: LYJ Patient Problem: Muscle Weakness Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CYBERONICS - HOUSTON PULSE GEN MODEL 1000 03/02/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 106 08/29/2022
LIVANOVA USA, INC. PULSE GEN MODEL 103 08/15/2022
LIVANOVA USA, INC. PULSE GEN MODEL 105 04/05/2022
LIVANOVA USA, INC. PULSE GEN MODEL 105 03/01/2022
CYBERONICS - HOUSTON LEAD MODEL 304 06/03/2021
LIVANOVA USA, INC. PULSE GEN MODEL 1000 05/14/2021
LIVANOVA USA, INC. PULSE GEN MODEL 106 04/16/2021
CYBERONICS - HOUSTON PULSE GEN MODEL 106 02/03/2021
LIVANOVA USA, INC. PULSE GEN MODEL 106 05/20/2020
-
-