
Imbiotechnologies
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OCCLUSIN 500 ARTIFICIAL EMBOLIZATION DEVICE is an FDA 510(k)-cleared medical device (K093813) manufactured by Imbiotechnologies. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 9, 2010. Regulation: 8.