• 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 
 > 
 
172 records meeting your search criteria returned- Product Code: LKK Product Problem: Failure to Disconnect Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 04/29/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 04/29/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 04/25/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 04/14/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 04/08/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 03/24/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 03/14/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 02/28/2022
MEDTRONIC NEUROMODULATION SYNCHROMED II 01/04/2022
MEDTRONIC NEUROMODULATION SYNCHROMED II 12/08/2021
-
-