
Innerspace, Inc.
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ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER is an FDA 510(k)-cleared medical device (K010422) 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 June 27, 2001. Regulation: 8.