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Pentacam AXL

Page Type
Cleared 510(K)
510(k) Number
K152311
510(k) Type
Traditional
Applicant
Oculus Optikgerate GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
159 days
Submission Type
Summary

Pentacam AXL

Page Type
Cleared 510(K)
510(k) Number
K152311
510(k) Type
Traditional
Applicant
Oculus Optikgerate GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/20/2016
Days to Decision
159 days
Submission Type
Summary