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 
 4 
 
 
31 records meeting your search criteria returned- Product Code: DRM Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION AUTOPULSE PLATFORM RESUSCITATION 10/03/2020
PHYSIO-CONTROL, INC. - 3015876 LUCAS CHEST COMPRESSION SYSTEM 12/01/2018
PHYSIO-CONTROL LUCAS 10/29/2018
JOLIFE AB LUCAS 3 CHEST COMPRESSION SYSTEM 01/09/2018
JOLIFE AB LUCAS 2 07/13/2016
JOLIFF AB LUCAS 2 CHEST COMPRESSION SYSTEM 03/04/2016
JOLIFE AB LUCAS(T) CPR CHEST COMPRESSION SYSTEM 09/09/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 06/22/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 02/25/2015
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 02/24/2015
-
-