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GDT-1000 System

Page Type
Cleared 510(K)
510(k) Number
K180096
510(k) Type
Traditional
Applicant
AcuVu Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2018
Days to Decision
90 days
Submission Type
Summary

GDT-1000 System

Page Type
Cleared 510(K)
510(k) Number
K180096
510(k) Type
Traditional
Applicant
AcuVu Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2018
Days to Decision
90 days
Submission Type
Summary