• 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 
 6 
 7 
 8 
 9 
 10 
 > 
 
127 records meeting your search criteria returned- Product Code: MCW Patient Problem: Embolism/Embolus Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CARDIOVASCULAR SYSTEMS, INC. (ABBOTT) DIAMONDBACK 360 PERIPHERAL ORBITAL ATHER 02/20/2024
CARDIOVASCULAR SYSTEMS, INC. DIAMONDBACK 360 PERIPHERAL ORBITAL ATHER 02/12/2024
CARDIOVASCULAR SYSTEMS INC. STEALTH 360 ORBITAL ATHERECTOMY SYSTEM 02/09/2024
BOSTON SCIENTIFIC CORPORATION JETSTREAM XC 02/06/2024
BOSTON SCIENTIFIC CORPORATION JETSTREAM ATHERECTOMY CATHETER 02/06/2024
CARDIOVASCULAR SYSTEMS, INC. STEALTH 360 ORBITAL ATHERECTOMY SYSTEM 02/02/2024
COVIDIEN BTK TURBOHAWK 01/23/2024
COVIDIEN HAWKONE 01/23/2024
ABBOTT VASCULAR NETHERLANDS DIAMONDBACK 360¿ ORBITAL ATHERECTOMY SYS 01/19/2024
CARDIOVASCULAR SYSTEMS, INC. (ABBOTT) DIAMONDBACK 360 PERIPHERAL ORBITAL ATHER 01/19/2024
-
-