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VS-VISIONSENSE STEREOSCOPIC VISION SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073279
510(k) Type
Special
Applicant
VISIONSENSE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2008
Days to Decision
105 days
Submission Type
Summary