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

PANCREATIC DRAINAGE TUBE

K Number: K021672 · Decision Apr 16, 2003
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
7
Review Days
330

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Basic Information

Device Name
PANCREATIC DRAINAGE TUBE
K Number
K021672
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aomori Olympus Co., Ltd.
Date Received
May 21, 2002
Decision Date
April 16, 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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K033333 SINGLE USE 3-LUMEN BALLOON CATHETER, MODELS B-230Q-A AND B-230Q-B
K031523 OLYMPUS ULTRASONIC SURGICAL SYSTEM
K031710 OLYMPUS ULTRASONIC SURGICAL SYSTEM
K022446 MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C