• 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 
 3 
 4 
 > 
 
34 records meeting your search criteria returned- Product Code: LIT Product Problem: Off-Label Use Report Date From: 01/1/2015
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT VASCULAR RX VIATRAC 14 PLUS PERIPHERAL DILATATION 12/20/2020
ABBOTT VASCULAR RX VIATRAC 14 PLUS PERIPHERAL DILATATION 12/20/2020
NUMED, INC. TYSHAK II CATHETER 11/03/2020
NUMED CANADA, INC. TYSHAK II CATHETER 10/14/2020
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 08/28/2020
ABBOTT VASCULAR RX VIATRAC 14 PLUS PERIPHERAL DILATION C 07/07/2020
ABBOTT VASCULAR RX VIATRAC PLUS 04/17/2020
ABBOTT VASCULAR VIATRAC 14 PLUS PERIPHERAL DILATATION CA 02/26/2020
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 02/12/2020
ABBOTT VASCULAR ARMADA 35 PTA CATHETER 01/23/2020
-
-