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 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
118 records meeting your search criteria returned- Product Code: LDD Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 12/09/2015
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 11/11/2015
PHILIPS MEDICAL SYSTEMS CODEMASTER XL+ 10/20/2015
PHILIPS MEDICAL SYSTEMS SWITCHED INTERNAL PADDLES - 7.5 CM 10/14/2015
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 10/03/2015
PHYSIO-CONTROL, INC HANDLES AND CONNECTOR WITH DISCHARGE CON 08/28/2015
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 08/28/2015
ZOLL ZOLL 08/26/2015
PHILIPS MEDICAL SYSTEMS CODEMASTER 100 08/19/2015
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 07/27/2015
-
-