
Power Medical Interventions, Inc.
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IDRIVES, IDRIVEC, IDRIVEF WITH VASCULAR INDICATIONS is an FDA 510(k)-cleared medical device (K073148) manufactured by Power Medical Interventions, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 2007. Regulation: 8.