Medical Device Manufacturer · US , Washington, Dc , DC

Activiews, Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2011
3
Total
3
Cleared
0
Denied

Activiews, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Washington, Dc, US.

Historical record: 3 cleared submissions from 2011 to 2012. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Activiews, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Activiews, Ltd.

3 devices
1-3 of 3
Cleared Apr 13, 2012
CT-GUIDE NEEDLE GUIDANCE SYSTEM
K120300 · JAK
Radiology · 73d
Cleared Nov 10, 2011
CT-GUIDE NEEDLE GUIDANCE SYSTEM
K113063 · JAK
Radiology · 27d
Cleared Jun 21, 2011
CT-GUIDE NEEDLE GUIDANCE SYSTEM
K110812 · JAK
Radiology · 90d
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