FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

ABSOLUTE .035 SELF-EXPANDING BILIARY STENT SYSTEM

K Number: K033393 · Decision Nov 10, 2003
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
71
Review Days
18

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Basic Information

Device Name
ABSOLUTE .035 SELF-EXPANDING BILIARY STENT SYSTEM
K Number
K033393
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Guidant Corp.
Date Received
October 23, 2003
Decision Date
November 10, 2003
Product Code
FGE
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FGE Stents, Drains And Dilators For The Biliary Ducts

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