ENDOSCOPE CONTOUR DETECTION DEVICE, MODEL 3DX45 AND COLONOSCOPE, MODEL XCF-Q140L/13D— 510(k) K002749

Name: FDA 510(k) clearance K002749
Creator: U.S. Food and Drug Administration
Published: 2000-12-04

Substantially Equivalent

The Olympus Optical Co.

FDA 510(k) clearance K002749 for ENDOSCOPE CONTOUR DETECTION DEVICE, MODEL 3DX45 AND COLONOSCOPE, MODEL XCF-Q140L/13D, Substantially Equivalent on 2000-12-04. Applicant: The Olympus Optical Co.. Device class: 2.

Clearance details

Applicant: The Olympus Optical Co.
Product code: Code FDF
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2000-09-05
Decision date: 2000-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FDF

product code FDF

Death: 8
Injury: 729
Malfunction: 61,773
Total: 62,510

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.