• 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 
 
 
19 records meeting your search criteria returned- Product Code: DRB Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 02/10/2017
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 02/10/2017
BIOTRONIK SE & CO. KG STYLET S 65-C 08/30/2016
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 05/25/2016
SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 12/18/2015
SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 12/18/2015
SPECTRANETICS SPECTRANETICS LEAD LOCKING DEVICE 06/23/2015
SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 06/13/2014
SPECTRANETICS CORPORATION SPECTRANETICS LEAD LOCKING DEVICE 02/06/2014
-
-