• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: NIQ Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND RESOLUTE ONYX RX 04/15/2019
MEDTRONIC IRELAND ENDEAVOR RESOLUTE RX 02/05/2019
MEDTRONIC IRELAND RESOLUTE ONYX RX 01/24/2019
MEDTRONIC IRELAND RESOLUTE ONYX RX 12/13/2018
MEDTRONIC IRELAND RESOLUTE ONYX RX 12/13/2018
MEDTRONIC IRELAND RESOLUTE ONYX RX 12/13/2018
MEDTRONIC IRELAND RESOLUTE ONYX RX 12/13/2018
MEDTRONIC IRELAND RESOLUTE ONYX RX 10/15/2018
MEDTRONIC IRELAND RESOLUTE ONYX RX 04/16/2018
BOSTON SCIENTIFIC - GALWAY PROMUS PREMIER¿ 04/12/2018
-
-