• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
51 records meeting your search criteria returned- Product Code: CCK Product Problem: Unable to Obtain Readings Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST PAUL BCI 08/20/2021
NIHON KOHDEN CORPORATION GF-210RA 04/15/2021
NIHON KOHDEN CORPORATION GF-210RA 04/15/2021
NIHON KOHDEN CORPORATION GF-210RA 01/27/2021
NIHON KOHDEN CORPORATION GF-210RA 11/16/2020
MINDY.FABER@VYAIRE.COM VITAL SIGNS¿ ADULT/PEDIATRIC AIRWAY ADAP 11/15/2020
NIHON KOHDEN CORPORATION GF-210RA 10/20/2020
NIHON KOHDEN CORPORATION GF-210RA 09/24/2020
NIHON KOHDEN CORPORATION GF-210RA 09/11/2020
TELEFLEX MEDICAL HUDSON CO2 SOFTECH CANNULA A, 14FT 14FT, 06/24/2020
-
-