• 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: NOU Product Problem: Capacitative Coupling Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RESMED LTD ASTRAL 150 - AMER 03/08/2023
RESMED LTD ASTRAL 150 - AMER 03/08/2023
RESMED LTD ASTRAL 100 SC - DEU 03/01/2023
RESMED LTD ASTRAL 150 - AMER 02/24/2023
RESMED LTD ASTRAL 150 - AMER 02/24/2023
RESMED LTD ASTRAL 100 - AMER 02/08/2023
RESMED LTD MAIN PCB (ASTRAL 150) - 90HPA 12/28/2022
RESMED LTD ASTRAL 150 - AMER 11/16/2022
RESMED LTD MAIN PCB (ASTRAL 150) - 90HPA 11/03/2022
-
-