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 
 
 
56 records meeting your search criteria returned- Product Code: KNW Product Problem: Unintended Movement Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BARD PERIPHERAL VASCULAR, INC. DRENCOR ENCOR DRIVER 04/18/2019
BARD PERIPHERAL VASCULAR, INC. ENCOR DRIVER 04/17/2019
BARD PERIPHERAL VASCULAR, INC. ENCOR ENSPIRE SYSTEM 04/17/2019
BARD PERIPHERAL VASCULAR, INC. ENCOR FOOT PEDAL 04/17/2019
HOLOGIC, INC. ATEC 04/05/2019
HOLOGIC, INC. BREVERA BIOPSY SYSTEM WITH CORLUMINA IMA 02/25/2019
-
-