
Medtronic, Inc.
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DLP SINGLE STAGE VENOUS CANNULA INFLATABLE CUFF is an FDA 510(k)-cleared medical device (K120987) manufactured by Medtronic, 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 June 5, 2012. Regulation: 8.