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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
137 records meeting your search criteria returned- Product Code: MJN Product Problem: Inflation Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LEMAITRE VASCULAR, INC PRUITT F3 CAROTID SHUNT 09/10/2021
LEMAITRE VASCULAR, INC PRUITT F3 CAROTID SHUNT 09/10/2021
MICRO THERAPEUTICS, INC. DBA EV3 HYPERFORM 08/04/2021
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 07/29/2021
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 07/01/2021
MICRO THERAPEUTICS, INC. DBA EV3 HYPERFORM 12/18/2020
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 10/14/2020
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 10/02/2020
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 10/02/2020
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 09/10/2020
-
-