• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 > 
 
76 records meeting your search criteria returned- Product Code: BZD Patient Problem: Pulmonary Hypertension Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RESPIRONICS, INC. DREAMSTATION AUTO CPAP 05/30/2022
RESPIRONICS, INC. REMSTAR PLUS CPAP 05/23/2022
RESPIRONICS, INC. REMSTAR PLUS CPAP 05/23/2022
RESPIRONICS, INC. DREAMSTATION AUTO CPAP 04/01/2022
RESPIRONICS, INC. DREAMSTATION AUTO BIPAP 03/23/2022
RESPIRONICS, INC DREAMSTATION AUTO CPAP 02/16/2022
RESPIRONICS,INC. DREAMSTATION AUTO CPAP 01/06/2022
RESPIRONICS, INC. DREAMSTATION AUTO CPAP 12/22/2021
RESPIRONICS, INC. REMSTAR PRO C-FLEX+ 11/07/2021
RESPIRONICS, INC. DREAMSTATION AUTO CPAP 10/29/2021
-
-