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

PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

K Number: K041796 · Decision Aug 3, 2004
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
13
Review Days
32

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Basic Information

Device Name
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
K Number
K041796
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Cordis Corporation
Date Received
July 2, 2004
Decision Date
August 3, 2004
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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