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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
325 records meeting your search criteria returned- Product Code: KRD Product Problem: Premature Activation Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION INTERLOCK 11/03/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK-35 10/19/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK 10/07/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK 10/06/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK-35 10/06/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK 09/28/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK 09/21/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK-35 09/01/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK-35 08/31/2021
BOSTON SCIENTIFIC CORPORATION INTERLOCK 08/18/2021
-
-