• 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 
 8 
 9 
 10 
 > 
 
105 records meeting your search criteria returned- Product Code: CCK Product Problem: Failure to Read Input Signal Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAREFUSION SD ALARIS SYSTEM 04/07/2023
CAREFUSION SD ALARIS SYSTEM 09/21/2022
ST PAUL BCI CAPNOCHECK SLEEP CAPNOGRAPH/OXIMETER 09/01/2022
CAREFUSION SD ALARIS SYSTEM 06/16/2022
CAREFUSION SD ALARIS SYSTEM 06/02/2022
CAREFUSION SD ALARIS SYSTEM 04/28/2022
CAREFUSION SD 8300 ALARIS ETCO2 MODULE 03/01/2022
CAREFUSION SD 8300 ALARIS ETCO2 MODULE 02/22/2022
CAREFUSION SD 8300 ALARIS ETCO2 MODULE 02/21/2022
CAREFUSION SD ALARIS SYSTEM 12/01/2021
-
-