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 
 > 
 
50 records meeting your search criteria returned- Product Code: DRM Patient Problem: No Information Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION, INC. ZOLL AUTOPULSE 06/06/2018
DEFIBTECH, L.L.C. LIFELINE ARM 04/16/2018
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 08/10/2017
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 07/17/2017
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 01/13/2017
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 01/13/2017
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 10/11/2016
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/05/2016
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/03/2016
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 08/01/2016
-
-