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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002749
510(k) Type
Traditional
Applicant
The Olympus Optical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2000
Days to Decision
90 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002749
510(k) Type
Traditional
Applicant
The Olympus Optical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/2000
Days to Decision
90 days
Submission Type
Summary