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

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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
175 records meeting your search criteria returned- Product Code: MJN Report Date From: 1/1/2023 Report Date To: 12/31/2023

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LEMAITRE VASCULAR, INC. PRUITT F3 07/12/2023
LEMAITRE VASCULAR, INC. PRUITT F3 07/12/2023
LEMAITRE VASCULAR, INC. PRUITT F3 07/12/2023
LEMAITRE VASCULAR, INC. PRUITT F3 07/12/2023
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 07/11/2023
THE SPECTRANETICS CORPORATION BRIDGE OCCLUSION BALLOON 07/10/2023
MICRO THERAPEUTICS, INC. DBA EV3 HYPERGLIDE 07/10/2023
EDWARDS LIFESCIENCES, PR FOGARTY OCCLUSION CATHETER 07/10/2023
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 07/07/2023
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 07/07/2023
-
-