FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERIZATION SETS

K Number: K905229 · Decision Jan 18, 1991
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
464
Applicant Total
110
Review Days
59

Basic Information

Device Name
LAPAROSCOPIC CHOLANGIOGRAPHY CATHETERIZATION SETS
K Number
K905229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
ARROW INTL., INC.
Date Received
November 20, 1990
Decision Date
January 18, 1991
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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