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OptosAdvance 4.0 Software

Page Type
Cleared 510(K)
510(k) Number
K162039
510(k) Type
Traditional
Applicant
Optos Plc
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/8/2017
Days to Decision
201 days
Submission Type
Summary

OptosAdvance 4.0 Software

Page Type
Cleared 510(K)
510(k) Number
K162039
510(k) Type
Traditional
Applicant
Optos Plc
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
2/8/2017
Days to Decision
201 days
Submission Type
Summary