OLV 1100; OLV 1200 PULSE OXIMETERS

OLV 1100; OLV 1200 PULSE OXIMETERS is an FDA 510(k)-cleared medical device (K881307) manufactured by Nihon Kohden America, 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 November 3, 1988. Regulation: 8.