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 
 > 
 
24 records meeting your search criteria returned- Product Code: DRM Patient Problem: Laceration(s) Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION AUTOPULSE® RESUSCITATION MODEL 100 10/16/2022
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 10/16/2022
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 11/10/2021
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 05/12/2021
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 05/12/2021
ZOLL CIRCULATION AUTOPULSE PLATFORM RESUSCITATION 10/03/2020
PHYSIO-CONTROL, INC. - 3015876 LUCAS CPR CHEST COMPRESSION SYSTEM 07/01/2020
JOLIFE AB - 3005445717 LUCAS 2 CPR CHEST COMPRESSION SYSTEM 05/07/2019
JOLIFE AB - 3005445717 LUCAS¿ 2 CPR CHEST COMPRESSION SYSTEM 12/07/2018
PHYSIO-CONTROL, INC. - 3015876 LUCAS¿ 2 CPR CHEST COMPRESSION SYSTEM 11/16/2018
-
-