
Smiths Medical Asd, Inc.
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PERIFUSE CATHETER is an FDA 510(k)-cleared medical device (K121525) manufactured by Smiths Medical Asd, 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 1, 2012. Regulation: 8.