• 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 
 > 
 
19 records meeting your search criteria returned- Product Code: HCG Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PENUMBRA, INC. POD PACKING COIL 06/21/2019
PENUMBRA, INC. RUBY COIL 06/21/2019
PENUMBRA, INC. POD4 08/17/2018
PENUMBRA, INC. POD3 08/17/2018
DEPUY SYNTHES (CODMAN) HELIPAQ CERECYTE COIL 06/14/2018
PENUMBRA, INC. POD4 05/24/2018
PENUMBRA, INC. RUBY COIL 03/07/2018
PENUMBRA, INC. POD4 08/24/2017
PENUMBRA, INC. RUBY COIL 04/04/2017
PENUMBRA, INC. RUBY COIL 04/04/2017
-
-