Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 
5 records meeting your search criteria returned- Product Code: PBL Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABIOMED, INC. IMPELLA CP 03/21/2018
ABIOMED, INC. IMPELLA 11/24/2017
ABIOMED INC. IMPELLA CP 05/22/2017
ABIOMED, INC IMPELLA CP 11/18/2016
ABIOMED, INC. IMPELLA CP 06/08/2016
-
-