
Accucore, Inc.
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PCI MODEL 2041-PC TELEMETRY MONITOR is an FDA 510(k)-cleared medical device (K901031) manufactured by Accucore, 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 May 16, 1990. Regulation: 8.

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