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CT-GUIDE NEEDLE GUIDANCE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120300
510(k) Type
Traditional
Applicant
ACTIVIEWS LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2012
Days to Decision
73 days
Submission Type
Summary

CT-GUIDE NEEDLE GUIDANCE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K120300
510(k) Type
Traditional
Applicant
ACTIVIEWS LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/13/2012
Days to Decision
73 days
Submission Type
Summary