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VISIONSENSE STEREOSCOPIC VISION SYSTEM (VS SYSTEM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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