Last synced on 14 November 2025 at 11:06 pm

SURGIVISIO Device

Page Type
Cleared 510(K)
510(k) Number
K221028
510(k) Type
Traditional
Applicant
Ecential Robotics
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/6/2022
Days to Decision
90 days
Submission Type
Summary

SURGIVISIO Device

Page Type
Cleared 510(K)
510(k) Number
K221028
510(k) Type
Traditional
Applicant
Ecential Robotics
Country
France
FDA Decision
Substantially Equivalent
Decision Date
7/6/2022
Days to Decision
90 days
Submission Type
Summary