FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

FUJINON COLONOSCOPE FOR DOUBLE BALLOON ENTERSCOPY SYSTEM MODEL, EC-450B15

K Number: K090116 · Decision Apr 22, 2009
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
111
Applicant Total
30
Review Days
91

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Basic Information

Device Name
FUJINON COLONOSCOPE FOR DOUBLE BALLOON ENTERSCOPY SYSTEM MODEL, EC-450B15
K Number
K090116
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fujinon, Inc.
Date Received
January 21, 2009
Decision Date
April 22, 2009
Product Code
FDF
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
FDF Colonoscope And Accessories, Flexible/Rigid

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Other Clearances by Fujinon, Inc.

K Number Device Name
K120446 FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2
K112391 FUJINON COLONOSCOPES
K102466 FUJINON EPX-4440HD DIGITAL VIDEO PROCESSOR
K111243 FUJINON ULTRASONIC PROCESSOR
K091773 FUJINON STERILE OVERTUBES
K063316 FUJINON MODEL EG-530N TRANS NASAL INSERTION
K063847 FUJINON ULTRASONIC ENDOSCOPE AND PROCESSOR, MODELS EG-530UR, EG-530UT AND SU-700
K050907 FUJINON G5 BRONCHOSCOPES, MODELS EB-470S, EB-250S, AND EB-270P
K042043 FUJINON INC. G5 GASTROSCOPES, MODELS EC-450WR5, EC-250WR5
K042076 FUJINON G5 DUODENSCOPES; G5 DUODENOSCOPES, ED-450XT5, ED-250XT5
Search all 30 clearances from Fujinon, Inc. →