• 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
 

 
 
8 records meeting your search criteria returned- Product Code: LYJ Patient Problem: Twitching 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 09/21/2021
LIVANOVA USA, INC. LEAD MODEL 302 06/30/2021
LIVANOVA USA, INC. PULSE GEN MODEL 102R 05/14/2021
LIVANOVA USA, INC. PULSE GEN MODEL 103 04/16/2021
LIVANOVA USA, INC. PULSE GEN MODEL 1000 03/22/2021
LIVANOVA USA, INC. LEAD MODEL 302 03/16/2021
LIVANOVA USA, INC. PULSE GEN MODEL 104 03/02/2021
LIVANOVA USA, INC. LEAD MODEL 304 08/26/2020
-
-