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
 

 
 
10 records meeting your search criteria returned- Product Code: IKZ Patient Problem: Low Oxygen Saturation Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARJOHUNTLEIGH, INC. ROTOPRONE 07/28/2020
ARJOHUNTLEIGH, INC. ROTOPRONE 01/07/2019
ARJOHUNTLEIGH, INC. ROTOPRONE 08/17/2018
ARJOHUNTLEIGH, INC. ROTOPRONE 04/26/2017
ARJOHUNTLEIGH, INC. ROTOPRONE 04/21/2017
ARJOHUNTLEIGH, INC. ROTOPRONE 04/21/2017
ARJOHUNTLEIGH POLSKA SP. Z O.O. ROTOPRONE 10/28/2016
ARJOHUNTLEIGH, INC. ROTOPRONE 10/04/2016
ARJOHUNTLEIGH INC. POTOPRONE 02/07/2014
ARJOHUNTLEIGH INC. ROTOPRONE 02/07/2014
-
-