• 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
 

 
 < 
 13 
 14 
 15 
 16 
 17 
 18 
 19 
 20 
 21 
 22 
 > 
 
493 records meeting your search criteria returned- Product Code: CBK Product Problem: Connection Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
VENTEC LIFE SYSTEMS, INC VOCSN 03/04/2023
VENTEC LIFE SYSTEMS, INC VOCSN 03/02/2023
VENTEC LIFE SYSTEMS, INC VOCSN 02/27/2023
VENTEC LIFE SYSTEMS, INC VOSCN 02/27/2023
VENTEC LIFE SYSTEMS, INC VOSCN 02/23/2023
VENTEC LIFE SYSTEMS, INC VOCSN 02/15/2023
VENTEC LIFE SYSTEMS, INC VOCSN 02/15/2023
VENTEC LIFE SYSTEMS, INC VOCSN 02/09/2023
VYAIRE MEDICAL VELA VENTILATOR 02/09/2023
VENTEC LIFE SYSTEMS, INC VOCSN 02/08/2023
-
-