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
 

 
 
9 records meeting your search criteria returned- Product Code: KDI Patient Problem: Swelling Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 09/17/2020
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 09/08/2020
OGDEN MANUFACTURING PLANT OPTIFLUX 160NRE DIALYZER FINISHED ASSY. 06/08/2020
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 01/30/2020
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 12/16/2019
BAXTER HEALTHCARE CORPORATION THERANOVA 400 11/06/2019
OGDEN MANUFACTURING PLANT OPTIFLUX 180NRE DIALYZER FINISHED ASSY. 10/01/2019
OGDEN MANUFACTURING PLANT OPTIFLUX 180NRE DIALYZER FINISHED ASSY. 10/01/2019
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 01/11/2019
-
-