• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
113 records meeting your search criteria returned- Product Code: CAW Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2014
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAIRE INC. OXYWELL 10/07/2016
CAIRE INC. OXYWELL 10/06/2016
CAIRE INC. NEWLIFE ELITE 09/29/2016
CAIRE INC. VISIONAIRE 09/29/2016
CAIRE INC. NEWLIFE ELITE 09/12/2016
CAIRE INC. NEWLIFE INTENSITY 10 09/12/2016
RESPIRONICS, INC. EVERFLO OXYGEN CONCENTRATOR 09/08/2016
CAIRE INC. AIRSEP NEWLIFE ELITE 09/02/2016
RESPIRONICS, INC. MILLENNIUM M10 OXYGEN CONCENTRATOR 08/10/2016
RESPIRONICS INC EVERFLO OXYGEN CONCENTRATOR 07/08/2016
-
-