Last synced on 9 May 2025 at 11:05 pm

CIRRUS™ HD-OCT Model 6000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233933
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2024
Days to Decision
155 days
Submission Type
Summary

CIRRUS™ HD-OCT Model 6000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233933
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2024
Days to Decision
155 days
Submission Type
Summary