
Philips Medical Systems
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COMPURECORD PERI-OPERATIVE ANESTHESIOLOGY INFORMATION SYSTEM is an FDA 510(k)-cleared medical device (K083413) manufactured by Philips Medical Systems. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 17, 2008. Regulation: 8.