• 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
 

 
 
10 records meeting your search criteria returned- Product Code: LNR Patient Problem: Swelling Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
THERAKOS CELLEX PHOTOPHERESIS SYSTEM 03/11/2020
THERAKOS, INC. / MALLINCRODT PHARMACEUTI CELLEX SYSTEM 10/31/2019
THERAKOS CELLEX PHOTOPHERESIS SYSTEM 05/04/2018
THERAKOS CELLEX PHOTOPHERESIS SYSTEM 12/08/2017
THERAKOS, INC CELLEX PHOTOPHERESIS SYSTEM 09/11/2017
THERAKOS, INC CELLEX PHOTOPHERESIS SYSTEM 07/18/2017
THERAKOS, INC CELLEX PHOTOPHERESIS SYSTEM 07/18/2017
THERAKOS, INC CELLEX PHOTOPHERESIS SYSTEM 07/01/2017
THERAKOS, INC THERAKOS CELLEX PHOTOPHERESIS SYSTEM 06/03/2016
THERAKOS INC. THERAKOS CELLEX PHOTOPHERESIS SYSTEM 02/06/2015
-
-