Last synced on 25 January 2026 at 3:41 am

CYSTOSCOPE, MODELS CE0004-C, CE006-C, CE3004-C, CE3027-C, CE7004-C, CE1204-C, CE1227-C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093725
510(k) Type
Traditional
Applicant
Canada Endoscope Corporation
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
8/30/2010
Days to Decision
270 days
Submission Type
Summary

CYSTOSCOPE, MODELS CE0004-C, CE006-C, CE3004-C, CE3027-C, CE7004-C, CE1204-C, CE1227-C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093725
510(k) Type
Traditional
Applicant
Canada Endoscope Corporation
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
8/30/2010
Days to Decision
270 days
Submission Type
Summary