CAPILLARY PERFUSION MONITOR #LD5000

CAPILLARY PERFUSION MONITOR #LD5000 is an FDA 510(k)-cleared medical device (K812005) manufactured by Nuclear Pacific, 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 February 3, 1982. Regulation: 8.