
Concentric Medical, Inc.
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HD GUIDE CATHETER, MODEL 90019, 90022, 90023, 90120, 90121, 90130, 90131 is an FDA 510(k)-cleared medical device (K091703) 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 October 13, 2009. Regulation: 8.