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

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
95 records meeting your search criteria returned- Product Code: LKK Patient Problem: Death Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION SYNCHROMED II 6837-40 03/01/2021
FLOWONIX MEDICAL, INC. PROMETRA II PROGRAMMABLE PUMP 06/09/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 05/13/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 03/03/2020
FLOWONIX MEDICAL, INC. PROMETRA II PROGRAMMABLE PUMP 12/16/2019
MEDTRONIC NEUROMODULATION IMPLANTABLE DRUG INFUSION PUMP 10/24/2019
MEDTRONIC NEUROMODULATION PUMP, INFUSION, IMPLANTED, PROGRAMMABLE 07/22/2019
CODMAN AND SHURTLEFF, INC MODEL 3000 - 30ML VOLUME, HIG 06/26/2019
MEDTRONIC NEUROMODULATION MEDTRONIC SYNCHROMED II PUMP 06/19/2019
FLOWONIX MEDICAL, INC PROMETRA PROGRAMMABLE PUMP 06/06/2019
-
-