• 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 
 > 
 
35 records meeting your search criteria returned- Product Code: LIT Product Problem: Device Handling Problem Report Date From: 01/1/2014
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
KANEKA CORPORATION METACROSS OTW PTA BALLOON DILATATION CAT 08/19/2019
Unknown Manufacturer OHICHO3 07/19/2019
KANEKA CORPORATION SENRI 07/09/2019
Unknown Manufacturer OHICHO3 06/27/2019
KANEKA SENRI 06/26/2019
KANEKA CORPORATION SHIDEN HP 06/04/2019
KANEKA CORPORATION SHIRANUI HP 04/24/2019
KANEKA CORPORATION RX-GENITY 11/07/2018
KANEKA CORPORATION OHICHO3 09/26/2018
KANEKA CORPORATION SENRI 08/29/2018
-
-