
Arrow Intl., Inc.
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ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD is an FDA 510(k)-cleared medical device (K011056) manufactured by Arrow Intl., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 23, 2001. Regulation: 8.