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

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
11 to 20 of 20 Results
ProductCode: FGE Applicant: COOK, INC. Decision Date To: 05/22/2024
 < 
 1 
 2 
 
Results per Page
New Search  
Export all 20 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
zilver 518 biliary stent COOK, INC. K033348 12/15/2003
modification to cook zilver biliary stent COOK, INC. K031821 07/18/2003
fanelli biliary stent COOK, INC. K010601 11/16/2001
cook zilver biliary stent COOK, INC. K010242 08/13/2001
mclean-stock percutaneous t-tube set COOK, INC. K921654 07/02/1992
gianturco-rosch biliary z stent COOK, INC. K921191 05/15/1992
cook-gianturco rosch biliary z-stent, modification COOK, INC. K903858 10/10/1990
cook-gianturco biliary z stent COOK, INC. K882610 04/21/1989
modified cope suture anchor COOK, INC. K873606 06/17/1988
greco-harvey surfactant bonded catheter for gastro COOK, INC. K851242 09/11/1985
-
-