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
 

 
 
9 records meeting your search criteria returned- Product Code: MHY Product Problem: Use of Incorrect Control/Treatment Settings Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION GENERATOR, DBS DUAL CHANNEL ACTIVA PC SN 06/02/2022
MEDTRONIC NEUROMODULATION GENERATOR, DBS PERCEPT PC 06/02/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 01/06/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 07/24/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 07/24/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 07/23/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 07/10/2018
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 07/10/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 06/08/2018
-
-