FDA 510(k) Applications Submitted by ACTIVIEWS LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110812 | 03/23/2011 | CT-GUIDE NEEDLE GUIDANCE SYSTEM | ACTIVIEWS LTD |
| K113063 | 10/14/2011 | CT-GUIDE NEEDLE GUIDANCE SYSTEM | ACTIVIEWS LTD |
| K120300 | 01/31/2012 | CT-GUIDE NEEDLE GUIDANCE SYSTEM | ACTIVIEWS LTD |
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