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Verza Guidance System

Page Type
Cleared 510(K)
510(k) Number
K160806
510(k) Type
Traditional
Applicant
CIVCO MEDICAL INSTRUMENTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2016
Days to Decision
134 days
Submission Type
Summary

Verza Guidance System

Page Type
Cleared 510(K)
510(k) Number
K160806
510(k) Type
Traditional
Applicant
CIVCO MEDICAL INSTRUMENTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2016
Days to Decision
134 days
Submission Type
Summary