
Idev Technologies, Inc.
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AKONYA ELIMINATOR MECHANICAL THROMBECTOMY DEVICE, MODEL EL 10060060 is an FDA 510(k)-cleared medical device (K030504) manufactured by Idev Technologies, 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 September 15, 2003. Regulation: 8.