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
 

 
 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
100 records meeting your search criteria returned- Product Code: MHY Patient Problem: Muscle Weakness Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/29/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/19/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/05/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. PERCEPT 12/02/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 11/17/2022
MEDTRONIC NEUROMODULATION ACTIVA 11/10/2022
MEDTRONIC IMPLANTABLE NEUROSTIMULATOR 11/06/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. PERCEPT 10/12/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 09/20/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 07/28/2022
-
-