• 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 
 5 
 6 
 7 
 > 
 
66 records meeting your search criteria returned- Product Code: MNS Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RESPIRONICS, INC. DREAMSTATION BIPAP ST30 12/22/2023
RESPIRONICS, INC. DREAMSTATION ST30 12/12/2023
RESPIRONICS, INC. DREAMSTATION ST30 12/11/2023
RESPIRONICS, INC. DREAMSTATION (ASV) 11/20/2023
RESPIRONICS, INC. DREAMSTATION ST30 11/02/2023
RESPIRONICS, INC. BIPAP AUTOSV ADV 11/01/2023
RESPIRONICS, INC. DREAMSTATION ST30 10/31/2023
RESPIRONICS, INC. DREAMSTATION ST30 10/06/2023
RESPIRONICS, INC. BIPAP A30 09/13/2023
RESPIRONICS, INC. DREAMSTATION BIPAP AUTOSV 08/28/2023
-
-