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

MODEIFICATION TO: SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

K Number: K031777 · Decision Jul 7, 2003
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
464
Applicant Total
315
Review Days
27

Basic Information

Device Name
MODEIFICATION TO: SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
K Number
K031777
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
CORDIS CORP.
Date Received
June 10, 2003
Decision Date
July 7, 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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