
Pathfinder Therapeutics, Inc.
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EXPLORER LIVER (PASSIVE TRACKING) is an FDA 510(k)-cleared medical device (K101979) manufactured by Pathfinder Therapeutics, 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 February 8, 2011. Regulation: 8.