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VISIO+CD VIEWER# KPSCDVE01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070606
510(k) Type
Traditional
Applicant
KEOSYS S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/24/2007
Days to Decision
50 days
Submission Type
Summary

VISIO+CD VIEWER# KPSCDVE01

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K070606
510(k) Type
Traditional
Applicant
KEOSYS S.A.S.
Country
France
FDA Decision
Substantially Equivalent
Decision Date
4/24/2007
Days to Decision
50 days
Submission Type
Summary