Innerspace, Inc.
ACT III VENTRICULAR CATHETER
SKU K013705UPC GWM
In Stock
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IIFDA 510(k) Cleared (K013705)
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Free shipping on orders over $99 · 30-day returns
Innerspace, Inc.
Free shipping on orders over $99 · 30-day returns
ACT III VENTRICULAR CATHETER is an FDA 510(k)-cleared medical device (K013705) manufactured by Innerspace, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 8, 2002. Regulation: 8.
