
Epimed International, Inc.
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FLEXIBLE INTRODUCER CANNULA, MODEL 135-1837 is an FDA 510(k)-cleared medical device (K051860) manufactured by Epimed International, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 21, 2005. Regulation: 8.