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Medrad Interventional/Possis
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ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001 is an FDA 510(k)-cleared medical device (K101406) manufactured by Medrad Interventional/Possis. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 15, 2010. Regulation: 8.