• 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
 

 
 
9 records meeting your search criteria returned- Product Code: HHM Patient Problem: Uterine Perforation Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HOLOGIC, INC SURESOUND 11/21/2019
HOLOGIC, INC SURESOUND 09/24/2019
HOLOGIC, INC. SURESOUND 11/08/2018
HOLOGIC, INC. SURESOUND 06/27/2018
HOLOGIC, INC SURESOUND 01/31/2017
HOLOGIC SURESOUND 10/31/2014
HOLOGIC SURESOUND 05/28/2014
HOLOGIC SURESOUND 03/20/2014
HOLOGIC SURESOUND 03/20/2014
-
-