• 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 
 3 
 4 
 5 
 6 
 > 
 
60 records meeting your search criteria returned- Product Code: OVB Patient Problem: Urinary Retention Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION SPACEOAR SYSTEM 05/03/2024
BOSTON SCIENTIFIC CORPORATION SPACEOAR VUE SYSTEM 04/18/2024
BOSTON SCIENTIFIC CORPORATION SPACEOAR VUE SYSTEM 04/05/2024
BOSTON SCIENTIFIC CORPORATION SPACEOAR SYSTEM 01/26/2024
BOSTON SCIENTIFIC CORPORATION SPACEOAR SYSTEM 12/11/2023
BOSTON SCIENTIFIC CORPORATION SPACEOAR SYSTEM 11/28/2023
BOSTON SCIENTIFIC CORPORATION SPACEOAR VUE SYSTEM 11/06/2023
BOSTON SCIENTIFIC CORPORATION SPACEOAR VUE SYSTEM 10/20/2023
BOSTON SCIENTIFIC CORPORATION SPACEOAR SYSTEM 10/02/2023
BOSTON SCIENTIFIC CORPORATION SPACEOAR VUE SYSTEM 09/28/2023
-
-