Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
185 records meeting your search criteria returned- Product Code: LKK Patient Problem: Underdose Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 11/13/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 11/13/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 11/03/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/28/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/28/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/27/2020
MDT PUERTO RICO OPERATIONS CO INDURA 10/15/2020
MEDTRONIC NEUROMODULATION SYNCHROMED II 10/01/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 08/30/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 08/11/2020
-
-