
Concentric Medical, Inc.
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CONCENTRIC GUIDE CATHETER, MODELS 90018, 90020 is an FDA 510(k)-cleared medical device (K003085) manufactured by Concentric Medical, 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 March 6, 2001. Regulation: 8.