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 
 > 
 
14 records meeting your search criteria returned- Product Code: MIP Product Problem: Insufficient Information Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 04/23/2016
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 08/12/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 07/16/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 07/16/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 01/12/2015
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 12/30/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 09/17/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 08/18/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 07/07/2014
AMERICAN MEDICAL SYSTEMS (MN) AMS ACTICON NEOSPHINCTER 02/15/2014
-
-