
Cma Microdialysis AB
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CMA CEREBRAL TISSUE MONITORING SYSTEM is an FDA 510(k)-cleared medical device (K020285) manufactured by Cma Microdialysis AB. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 22, 2002. Regulation: 8.