• 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
 

 
 < 
 1 
 2 
 3 
 4 
 > 
 
32 records meeting your search criteria returned- Product Code: LDD Product Problem: Failure to Deliver Energy Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHYSIO-CONTROL, INC HANDLES AND CONNECTOR WITH DISCHARGE CON 08/28/2015
PHYSIO-CONTROL, INC HANDLES AND CONNECTOR WITH DISCHARGE CON 05/20/2015
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 11/25/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 10/17/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 10/13/2014
PHYSIO-CONTROL, INC. LIFEPAK INTERNAL DEFIBRILLATOR CABLE/PAD 10/06/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 09/26/2014
PHYSIO-CONTROL, INC INTERNAL DEFIBRILLATION PADDLES 09/17/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 09/15/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 08/25/2014
-
-