• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
109 records meeting your search criteria returned- Product Code: BZD Patient Problem: Arrhythmia Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS / RESPIRONICS, INC. RESPIRONICS DREAMMACHINE CPAP 05/13/2022
RESPIRONICS, INC. DREAMSTATION AUTO CPAP 03/16/2022
RESPIRONICS, INC. DREAMSTATION AUTO CPAP 03/11/2022
RESPIRONICS, INC. DREAMSTATION CPAP 03/09/2022
RESPIRONICS INC. DREAMSTATION AUTO CPAP 03/08/2022
RESPIRONICS, INC. FITPACK, DREAMWEAR FULL, MED. FRAME, GBL 03/04/2022
RESPIRONICS, INC. DREAMSTATION AUTO 03/01/2022
RESPIRONICS, INC DREAMSTATION AUTO CPAP 02/01/2022
PHILIPS / RESPIRONICS, INC. PHILIPS CPAP DREASTATION 01/14/2022
RESPIRONICS, INC. DREAMSTATION AUTO CPAP 01/04/2022
-
-