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Invamed Technologies, Inc.
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SPPRO ESP, MODELS ESP 603-18-05, ESP 603-18-09 is an FDA 510(k)-cleared medical device (K032981) manufactured by Invamed Technologies, 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 21, 2004. Regulation: 8.