SYSTEM 7300 PULSE OXIMETER

SYSTEM 7300 PULSE OXIMETER is an FDA 510(k)-cleared medical device (K910521) manufactured by Advanced Medical Instruments, 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 April 17, 1991. Regulation: 8.