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 
 6 
 7 
 8 
 > 
 
78 records meeting your search criteria returned- Product Code: LDD Product Problem: Failure to Deliver Shock/Stimulation Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SCHILLER AG TEMPUS LS-MANUAL 03/24/2023
SCHILLER AG TEMPUS LS 03/24/2023
SCHILLER AG TEMPUS LS 03/23/2023
SCHILLER AG TEMPUS LS-MANUAL 03/08/2023
SCHILLER AG TEMPUS LS-MANUAL 02/06/2023
SCHILLER AG TEMPUS LS-MANUAL 01/24/2023
PHYSIO-CONTROL, INC. - 3015876 HANDLES & CONNECTOR WITH DISCHARGE CONTR 01/13/2023
ZOLL MEDICAL CORPORATION AUTOCLAVABLE INTERNAL HANDLES (MSERIES) 01/09/2023
ZOLL MEDICAL CORPORATION ASSY, PADDLES, ENG 12/21/2022
ZOLL MEDICAL CORPORATION ASSY, PADDLES, ENG 12/20/2022
-
-