Last synced on 23 May 2025 at 11:06 pm

CT-GUIDE NEEDLE GUIDANCE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110812
510(k) Type
Traditional
Applicant
ACTIVIEWS LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2011
Days to Decision
90 days
Submission Type
Summary

CT-GUIDE NEEDLE GUIDANCE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K110812
510(k) Type
Traditional
Applicant
ACTIVIEWS LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/21/2011
Days to Decision
90 days
Submission Type
Summary