Last synced on 25 January 2026 at 3:41 am

ALTIUS OCT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033961
510(k) Type
Special
Applicant
Interpore Cross Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2004
Days to Decision
114 days
Submission Type
Summary

ALTIUS OCT SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033961
510(k) Type
Special
Applicant
Interpore Cross Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/14/2004
Days to Decision
114 days
Submission Type
Summary