• 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 
 > 
 
14 records meeting your search criteria returned- Product Code: DRB Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MPRI STYLET KIT 07/15/2020
MPRI STYLET KIT 07/15/2020
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 09/17/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 08/05/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 05/29/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 03/04/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 01/11/2019
THE SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 01/03/2019
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 02/19/2018
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 09/08/2017
-
-