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Invivo Research, Inc.
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MODULAR TELEMETRY SYSTEM FOR THE VISION TELEPAK, MODEL 20701 is an FDA 510(k)-cleared medical device (K043354) manufactured by Invivo Research, 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 January 9, 2005. Regulation: 8.