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 
 > 
 
45 records meeting your search criteria returned- Product Code: NIQ Patient Problem: Pericardial Effusion Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND RESOLUTE ONYX RX 02/24/2022
ABBOTT VASCULAR XIENCE XPEDITION EVEROLIMUS ELUTING CORO 09/28/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY XD 09/17/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY 01/26/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY 01/25/2021
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 12/09/2020
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 11/13/2020
ABBOTT VASCULAR XIENCE DRUG ELUTING CORONARY STENT 10/08/2020
ABBOTT VASCULAR XIENCE SIERRA 09/02/2020
BOSTON SCIENTIFIC CORPORATION SYNERGY 03/12/2020
-
-