Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 
10 records meeting your search criteria returned- Product Code: MNT Patient Problem: Cardiac Arrest Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RESPIRONICS, INC. RESPIRONICS 04/09/2024
RESPIRONICS CALIFORNIA, LLC RESPIRONICS 07/06/2022
RESPIRONICS CALIFORNIA, LLC RESPIRONICS 06/23/2022
PHILIPS HEALTHCARE / RESPIRONICS, INC. BIPAP 06/02/2022
RESPIRONICS CALIFORNIA, LLC RESPIRONICS 04/20/2022
RESPIRONICS CALIFORNIA, LLC RESPIRONICS 09/15/2021
RESPIRONICS CALIFORNIA, LLC RESPIRONICS 05/12/2021
Unknown Manufacturer STELLAR 150 EUROPE GRP1 05/05/2021
Unknown Manufacturer STELLAR 150 EUROPE GRP1 05/05/2021
Unknown Manufacturer RESPIRONICS 04/16/2021
-
-