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

Import Refusal Report

  • Print
  • Share
  • E-mail
-

Refusal Details as Recorded in OASIS by FDA

for Refusal FR1-0013729-3/3/1


Manufacturer FEI3007482089
Manufacturer NameMiyuki Elex Co.,Ltd  
Manufacturer Address line 17-2-16,  
Manufacturer Address line 2  
Manufacturer's CityOsaka 579-8013  
Manufacturer Province/State  
Manufacturer Country/AreaJapan  
Product Code80FRN  
Importer's Product DescriptionINFUSION PUMP FOR EXPORT ONLY  
Refusal Date04-Mar-2011  
FDA DistrictFLA-DO  
Entry/doc/line/sfx FR1-0013729-3/3/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Charge(s)
Violation Code Section Charge Statement
NO 510(K)   801(a)(3); 502(o) Misbranding   It appears that a notice or other information respecting the device was not provided to FDA, as required by Section 510(k) and the device was not found to be substantially equivalent to a predicate device.  
-
-