• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARROW INTERNATIONAL LLC REDIGUARD IAB: 8FR 40CC 07/03/2023
ARROW INTERNATIONAL LLC ULTRAFLEX IAB: 7.5FR 40CC 06/29/2023
ARROW INTERNATIONAL LLC ML 2012, AFIB, HT N, CAD, HLD, HFREF 15% 06/26/2023
ARROW INTERNATIONAL LLC ULTRAFLEX IAB: 8FR 50CC 06/08/2023
ARROW INTERNATIONAL LLC ULTRAFLEX IAB: 7.5FR 40CC 06/08/2023
ARROW INTERNATIONAL LLC FIBEROPTIX ULTRA 8 IAB: 8FR 30CC 06/07/2023
ARROW INTERNATIONAL, LLC (SUBSIDIARY OF ARROW REDIGUARD IABP CATHETER 06/02/2023
ARROW INTERNATIONAL LLC ARROW INTRA-AORTIC BALLOON CATHETER 05/26/2023
ARROW INTERNATIONAL LLC ULTRAFLEX IAB: 7.5FR 40CC 05/16/2023
ARROW INTERNATIONAL LLC FIBEROPTIX ULTRA 8 IAB: 8FR 40CC 05/11/2023
-
-