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

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 
 > 
 
29 records meeting your search criteria returned- Product Code: DRM Patient Problem: Injury Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION AUTOPULSE® PLATFORM RESUSCITATION 10/18/2019
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 08/16/2019
ZOLL CIRCULATION INC AUTOPULSE® RESUSCITATION MODEL 100 04/30/2019
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 04/30/2019
ZOLL CIRCULATION, INC. AUTOPULSE® RESUSCITATION MODEL 100 03/21/2019
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 11/27/2018
ZOLL CIRCULATION AUTOPULSE® PLATFORM RESUSCITATION 11/09/2018
PHYSIO-CONTROL LUCAS 10/29/2018
ZOLL CIRCULATION AUTOPULSE® PLATFORM RESUSCITATION 10/12/2018
DEFIBTECH, L.L.C. LIFELINE 08/22/2017
-
-