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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
430 records meeting your search criteria returned- Product Code: DQA Report Date From: 1/1/2020 Report Date To: 12/31/2020

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAREFUSION SD 8220 ALARIS SPO2 - MASSIMO 12/01/2020
MEDIANA CO. LTD. NELLCOR 11/30/2020
NELLCOR PURITAN BENNETT MEXICO SA NELLCOR 11/30/2020
CAREFUSION SD 8210 ALARIS SPO2 - NELLCOR 11/29/2020
CAREFUSION SD 8220 ALARIS SPO2 - MASSIMO 11/28/2020
MASIMO CORPORATION PULSE OXIMETRY SENSOR 11/27/2020
CAREFUSION SD 8220 ALARIS SPO2 - MASSIMO 11/27/2020
CAREFUSION SD 8210 ALARIS SPO2 - NELLCOR 11/25/2020
CAREFUSION SD ALARIS SPO2- NELLCOR 11/25/2020
MEDLINE RENEWAL LNCS NEONATAL PROBE 11/25/2020
-
-