Last synced on 14 November 2025 at 11:06 pm

VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K082667
510(k) Type
Traditional
Applicant
VISIONSENSE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2008
Days to Decision
48 days
Submission Type
Summary

VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)

Page Type
Cleared 510(K)
510(k) Number
K082667
510(k) Type
Traditional
Applicant
VISIONSENSE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2008
Days to Decision
48 days
Submission Type
Summary