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
 

 
 
10 records meeting your search criteria returned- Product Code: DSR Patient Problem: Hematoma Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CVRX, INC. BAROSTIM NEO2 02/15/2024
CVRX, INC. BAROSTIM NEO2 08/01/2023
CVRX, INC. BAROSTIM NEO 05/24/2023
CVRX, INC. BAROSTIM NEO2 04/26/2023
CVRX, INC. BAROSTIM NEO 04/06/2023
CVRX, INC. BAROSTIM NEO 11/08/2022
CVRX, INC. BAROSTIM NEO 08/19/2022
CVRX, INC. BAROSTIM NEO 06/14/2022
CVRX, INC. BAROSTIM NEO 06/02/2022
CVRX, INC. BAROSTIM NEO 12/15/2021
-
-