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 
 > 
 
120 records meeting your search criteria returned- Product Code: LKK Patient Problem: Dyspnea Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/24/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/22/2019
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 10/14/2019
MDT PUERTO RICO OPERATIONS CO SYNCHROMED II 10/11/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 10/04/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 09/30/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 09/03/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 08/21/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. SYNCHROMED II 08/07/2019
MEDTRONIC PUERTO RICO OPERATIONS CO., JU SYNCHROMED II 08/02/2019
-
-