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

FUSE 1C COLONOSCOPY SYSTEM

K Number: K132839 · Decision Feb 6, 2014
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
111
Applicant Total
27
Review Days
149

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Basic Information

Device Name
FUSE 1C COLONOSCOPY SYSTEM
K Number
K132839
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endochoice, Inc.
Date Received
September 10, 2013
Decision Date
February 6, 2014
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

Similar 510(k) Clearances

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Other Clearances by Endochoice, Inc.

K Number Device Name
K160275 Fuse Endoscopic System with FuseBox Processor
K161482 EndoChoice Water Bottle Cap Irrigation System
K161167 Seal Single-Use Biopsy Valve
K160403 SmartStart Air/Water and Suction Valves
K153588 EndoChoice Water Bottle Cap System
K151475 EndoChoice Select Injection Needle
K152182 Fuse Gastroscopy System
K152580 rescuenet
K142155 ENDOCHOICE WATER BOTTLE CAP SYSTEM
K140472 BONASTENT TRACHEAL / BRONCHIAL
Search all 27 clearances from Endochoice, Inc. →