Activiews, Ltd.
CT-GUIDE NEEDLE GUIDANCE SYSTEM
SKU K120300UPC JAK
In Stock
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IIFDA 510(k) Cleared (K120300)
1
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Activiews, Ltd.
Free shipping on orders over $99 · 30-day returns
CT-GUIDE NEEDLE GUIDANCE SYSTEM is an FDA 510(k)-cleared medical device (K120300) manufactured by Activiews, Ltd.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 12, 2012. Regulation: 8.
