
Creative Care Systems, Inc.
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DAYPAK SYS VII CATHETER CARE KIT is an FDA 510(k)-cleared medical device (K840919) manufactured by Creative Care Systems, 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 April 16, 1984. Regulation: 8.

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