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
 

 
 < 
 1 
 2 
 3 
 4 
 > 
 
36 records meeting your search criteria returned- Product Code: GKP Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INSTRUMENTATION LABORATORY ACL TOP CTS 09/20/2017
INSTRUMENTATION LABORATORY ACL TOP 500 CTS 09/11/2017
SYSMEX RA CO., LTD. SYSMEX CA-660 03/23/2017
INSTRUMENTATION LABORATORY - BEDFORD HEMOSIL RINSE SOLUTION 4L 11/29/2016
INSTRUMENTATION LABORATORY - BEDFORD ACL TOP 300 CTS 11/21/2016
INSTRUMENTATION LABORATORY - BEDFORD ACL TOP 500 CTS 10/28/2016
INSTRUMENTATION LABORATORY - BEDFORD ACL TOP 500 CTS 10/07/2016
SYSMEX CORPORATION SYSMEX CA-1500 07/19/2016
SYSMEX CORPORATION SYSMEX CA-660 06/29/2016
SYSMEX CORPORATION CA-1500 CP 04/20/2016
-
-