
Marquette Electronics, Inc.
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SERIES 7000 END TIDAL CO2 MONITORING SYSTEM is an FDA 510(k)-cleared medical device (K851001) manufactured by Marquette Electronics, 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 May 12, 1985. Regulation: 8.

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