• 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
 

 
 
 1 
 2 
 3 
 4 
 > 
 
34 records meeting your search criteria returned- Product Code: MNT Product Problem: Occlusion Within Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 05/27/2018
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 04/25/2018
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 01/10/2018
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 11/13/2017
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 10/16/2017
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 06/19/2017
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 06/13/2017
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 05/01/2017
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 04/14/2017
RESPIRONICS CALIFORNIA, INC V60 VENTILATOR 04/06/2017
-
-