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

ENDOSCOPE CONTOUR DETECTION DEVICE, MODEL 3DX45 AND COLONOSCOPE, MODEL XCF-Q140L/13D

K Number: K002749 · Decision Dec 4, 2000
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
111
Applicant Total
22
Review Days
90

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Basic Information

Device Name
ENDOSCOPE CONTOUR DETECTION DEVICE, MODEL 3DX45 AND COLONOSCOPE, MODEL XCF-Q140L/13D
K Number
K002749
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Olympus Optical Co.
Date Received
September 5, 2000
Decision Date
December 4, 2000
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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