
Guidant Corporation
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CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020 is an FDA 510(k)-cleared medical device (K041574) manufactured by Guidant Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 11, 2004. Regulation: 8.

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