• 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
 

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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LIVANOVA USA, INC. PULSE GEN MODEL UNK 10/13/2023
LIVANOVA USA, INC. PULSE GEN MODEL 1000 10/09/2023
CYBERONICS - HOUSTON PULSE GEN MODEL 106 03/28/2023
LIVANOVA USA, INC. PULSE GEN MODEL 1000 05/26/2022
CYBERONICS - HOUSTON PULSE GEN MODEL 104 04/29/2022
Unknown Manufacturer PULSE GEN MODEL 1000 06/28/2021
LIVANOVA USA, INC. PULSE GEN MODEL 102 06/10/2021
-
-