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
 

 
 
8 records meeting your search criteria returned- Product Code: MCX Patient Problem: Dyspnea Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CARDIOVASCULAR SYSTEMS, INC. DIAMONDBACK CORONARY ORBITAL ATHERECTOMY 11/17/2020
CARDIOVASCULAR SYSTEMS, INC. DIAMONDBACK 360 CORONARY ORBITAL ATHEREC 09/18/2020
CARDIOVASCULAR SYSTEMS, INC. DIAMONDBACK 360 CORONARY ORBITAL ATHEREC 07/23/2020
BOSTON SCIENTIFIC - COSTA RICA (COYOL) ROTAWIRE¿ AND WIRECLIP¿ TORQUER 11/28/2016
BOSTON SCIENTIFIC - CORK ROTALINK¿ PLUS 11/28/2016
BOSTON SCIENTIFIC - CORK ROTALINK¿ ADVANCER 09/15/2015
BOSTON SCIENTIFIC - CORK ROTALINK¿ BURR 09/15/2015
BOSTON SCIENTIFIC - COSTA RICA (HEREDIA) ROTAWIRE¿ AND WIRECLIP¿ TORQUER 09/15/2015
-
-