SENSOCOR TM R-TEST 24OXL

SENSOCOR TM R-TEST 24OXL is an FDA 510(k)-cleared medical device (K894234) manufactured by Sensocor. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 2, 1989. Regulation: 8.