Last synced on 14 November 2025 at 11:06 pm

AT 030

Page Type
Cleared 510(K)
510(k) Number
K180839
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/7/2018
Days to Decision
69 days
Submission Type
Summary

AT 030

Page Type
Cleared 510(K)
510(k) Number
K180839
510(k) Type
Traditional
Applicant
Carl Zeiss Meditec AG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/7/2018
Days to Decision
69 days
Submission Type
Summary