510(k) K031821

Device
MODIFICATION TO COOK ZILVER BILIARY STENT
Applicant
Cook, Inc.
510(k) number
K031821
Product code
FGE
Decision
Unknown (SESU)
Decision date
2003-07-18
Date received
2003-06-13
Regulation
876.5010
Classification name
Stents, Drains And Dilators For The Biliary Ducts
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
CAROL ZWISSLER
Address
750 Daniels Way P.O. Box 489 Bloomington IN US 47402 47402

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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